Monthly Archives: August 2017

SHAREHOLDER ALERT: Pomerantz Law Firm Reminds Shareholders with Losses on their Investment in Arconic, Inc. of Class Action Lawsuit and Upcoming Deadline – ARN

NEW YORK, NY / ACCESSWIRE / August 29, 2017 / Pomerantz LLP announces that a class action lawsuit has been filed against Arconic, Inc. (“Arconic” or the “Company”) (NYSE: ARNC) and certain of its officers. The class action, filed in United States District Court, Southern District of New York, and docketed under 17-cv-05312, is on behalf of a class consisting of investors who purchased or otherwise acquired Arconic securities, seeking to recover compensable damages caused by defendants’ violations of the Securities Exchange Act of 1934.

If you are a shareholder who purchased Arconic securities between February 28, 2017, and June 26, 2017, both dates inclusive, you have until September 11, 2017, to ask the Court to appoint you as Lead Plaintiff for the class. A copy of the Complaint can be obtained at www.pomerantzlaw.com. To discuss this action, contact Robert S. Willoughby at rswilloughby@pomlaw.com or 888.476.6529 (or 888.4-POMLAW), toll-free, Ext. 9980. Those who inquire by e-mail are encouraged to include their mailing address, telephone number, and the number of shares purchased.

[Click here to join this class action]

Arconic Inc. is a global provider of lightweight multi-material solutions, focused on the aerospace market in addition to serving the automotive, industrial gas turbine, commercial transportation, and building and construction markets. The Company also provides titanium, aluminum, nickel-based super alloy, and specialty alloy solutions.

The Complaint alleges that throughout the Class Period, Defendants made materially false and misleading statements regarding the Company’s business, operational and compliance policies. Specifically, Defendants made false and/or misleading statements and/or failed to disclose that: (i) Arconic knowingly supplied its highly flammable Reynobond PE (polyethylene) cladding panels for use in construction; (ii) the foregoing conduct significantly increased the risk of property damage, injury and/or death in buildings constructed with Arconic’s Reynobond PE panels; and (iii) as a result of the foregoing, Arconic’s public statements were materially false and misleading at all relevant times.

On June 14, 2017, a fire broke out at the 24-story Grenfell Tower apartment block in London. The fire burned for roughly 60 hours, destroying the building and causing at least 80 deaths and over 70 injuries.

On June 24, 2017, The New York Times published an article entitled “Why Grenfell Tower Burned: Regulators Put Cost Before Safety’, describing the causes of the Grenfell Tower fire and attributing the rapid spread of the fire to highly flammable Reynobond PE cladding panels manufactured by Arconic and used in the building’s construction.

On that same day, Reuters published an article entitled “Arconic knowingly supplied flammable panels for use in tower: emails,” revealing that Arconic sales managers were aware that flammable panels would be distributed for use at Grenfell Tower.

On June 26, 2017, Arconic issued a press release announcing it would discontinue global sales of Reynobond PE for use in high-rise buildings after the material was suspected to have contributed to the spread of the deadly fire at the Grenfell Tower apartment complex in London.

On these disclosures, Arconic’s common share price fell $3.70, or 14.49%, to close at $21.84 on June 27, 2017.

The Pomerantz Firm, with offices in New York, Chicago, Florida, and Los Angeles, is acknowledged as one of the premier firms in the areas of corporate, securities, and antitrust class litigation. Founded by the late Abraham L. Pomerantz, known as the dean of the class action bar, the Pomerantz Firm pioneered the field of securities class actions. Today, more than 80 years later, the Pomerantz Firm continues in the tradition he established, fighting for the rights of the victims of securities fraud, breaches of fiduciary duty, and corporate misconduct. The Firm has recovered numerous multimillion-dollar damages awards on behalf of class members. See www.pomerantzlaw.com

SOURCE: Pomerantz LLP

ReleaseID: 474094

Plaintree Systems Inc Releases Fiscal 2017 Audited Results and Q1-2018 Unaudited Interim Results

ARNPRIOR, ON / ACCESSWIRE / August 29, 2017 / Plaintree Systems Inc. (the ”Company”) (OTC PINK: PTEEF) CSE: NPT), is pleased to report it has filed its audited consolidated financial statements and management discussion and analysis for the year ended March 31, 2017. Further, the Company has also filed its interim consolidated financial statements and management discussion and analysis for the three (3) months ended June 30, 2017.

As announced on July 28, 2017, the Company was delayed in issuing its annual financial statements and management discussion and analysis for the 2017 fiscal year which were due to be released on July 31, 2017. Pursuant to the wording of the management cease trade order issued by the Ontario Securities Commission on August 1, 2017, the order will be revoked two business days following the filing of the annual 2017 and Q1 2018 financial statements and corresponding management discussion and analysis, which date will be August 31, 2017. As of August 31, 2017 the prior restrictions on the trading of the Company’s securities by the CEO and CFO as set out in the order will be removed.

Annual 2017

For the year ended March 31, 2017, the Company posted a loss of $2,639,634 on revenue of $12,844,110 as compared to a loss of $2,258,584 on revenue of $15,746,175 for the 2016 year.

Q1 2018

For the first three months of fiscal 2018, the Company posted net earnings of $352,763 on revenue of $3,616,516 and as compared to a loss of $149,253 on revenue of $3,432,531 for Q1 2017.

David Watson, the Company’s President and Chief Executive Officer stated, ”The biggest subsidiary in Plaintree is Triodetic and one of its main product lines is the engineering and manufacture of foundations for buildings installed on unstable soils such as permafrost, clay and also areas prone to flooding. With the global environmental instability the world now faces, sales of these foundations are experiencing strong growth. This increase in foundation orders combined with improved sales and margins on all of Plaintree’s other product lines resulted in this profitable quarter. Also, the sale by the Company of the business of Arnprior Fire Trucks (announced on June 6, 2017) and the discontinuation of this business has also freed up much needed capital to help grow the Company’s more productive divisions.”

About Plaintree Systems Inc.

Plaintree has two diversified product lines consisting of Specialty Structures and Electronics. The Specialty Structures Division includes the former Triodetic Group with over 40 years of experience, is a design/build manufacturer of steel, aluminum and stainless steel specialty structures such as commercial domes, free form structures, barrel vaults, space frames and industrial dome coverings, Spotton Corporation, a design and manufacturer of high end custom hydraulic and pneumatic valves and cylinders and the recently acquired Madawaska Doors, a design and manufacturer of premium solid wood doors. The Electronics Division includes the legacy Hypernetics, Summit Aerospace USA Inc. and Plaintree free space optics (FSO) businesses. Plaintree’s FSO systems transmit data at high speeds using beams of light instead of traditional radio frequency which can suffer from congestion. Hypernetics was established in 1972 and is a manufacturer of avionic components for various applications including aircraft antiskid braking, aircraft instrument indicators, solenoids, high purity valves and permanent magnet alternators. Summit Aerospace USA Inc. provides high precision machining to the aerospace and defense markets. Our facility includes 5 axis CNC precision machining of complex castings and large ring parts such as turbine and assembly shrouds as well as assembly & pressure seals. Summit will support requirements from concept, prototype and throughout production.

Plaintree’s shares are traded under the symbol ”NPT”. Shareholders and Investors can access Company information on CSE’s website and receive full Company disclosure monthly. For more information on Plaintree or to receive stock quotes, complete with trading summaries, bid size and ask price, brokerage house participation, insider reports, news releases, disclosure information, and CSE and SEDAR filings, visit the CSE website at www.cnsx.ca or the Company’s website at www.plaintree.com.

Plaintree is publicly traded in Canada on the CSE (NPT) with 12,925,253 common shares and 18,325 class A preferred shares outstanding.

This press release may include statements that are forward-looking and based on current expectations. The actual results of the company may differ materially from current expectations. The business of the company is subject to many risks and uncertainties, including changes in markets for the company’s products, delays in product development and introduction to manufacturing and intense competition. For a more detailed discussion of the risks and uncertainties related to the Company’s business, please refer to documents filed by the company with the Canadian regulatory authorities, including the annual report of the Company for the fiscal year ended March 31, 2017 and related management discussion and analysis. Canadian Securities Exchange has not reviewed and does not accept responsibility for the adequacy or accuracy of the content of this news release.

For further information: (613) 623-3434 x2261

SOURCE: Plaintree Systems Inc.

ReleaseID: 474104

EQUITY ALERT: Levi & Korsinsky, LLP Notifies Shareholders of Foundation Medicine, Inc. of a Class Action Lawsuit and a Lead Plaintiff Deadline of September 26, 2017 – FMI

NEW YORK, NY / ACCESSWIRE / August 29, 2017 / The following statement is being issued by Levi & Korsinsky, LLP:

To: All persons or entities who purchased
or otherwise acquired securities of Foundation Medicine, Inc. (”Foundation”) (NASDAQ: FMI) between
February 26, 2014 and November 3, 2015. You are hereby notified that a securities class action lawsuit has been commenced in the USDC for the District of Massachusetts. To get more information go to:

http://www.zlk.com/pslra-sbm/foundation-medicine-inc?wire=1

or contact Joseph E. Levi, Esq. either via email at jlevi@levikorsinsky.com or by telephone at (212) 363-7500, toll-free: (877) 363-5972. There is no cost or obligation to you.

The complaint alleges that throughout the class period Defendants issued materially false and/or misleading statements and/or failed to disclose material information regarding: (1) the reimbursement process and likelihood of coverage for Foundation’s tumor tests by Medicare; and (2) the Company’s financial guidance. As a result of these false statements, Foundation common stock traded at artificially inflated prices during the Class Period.

On July 29, 2015, the Company disclosed that it was not making the strides obtaining coverage it had claimed to have been making during the Class Period, and that Foundation would receive no Medicare payments in 2015 for its tumor profiling tests due to a delay in receiving a local coverage determination from its regional Medicare Administrative Contractor. As a result of the delay, the Company slashed its 2015 financial guidance. Then, on November 3, 2015, the Company disclosed a further revision to the already reduced number of clinical tests it expected to report for 2015.

If you suffered a loss in Foundation you have until September 26, 2017 to request that the Court appoint you as lead plaintiff. Your ability to share in any recovery doesn’t require that you serve as a lead plaintiff.

Levi & Korsinsky is a national firm with offices in New York, California, Connecticut, and Washington D.C. The firm’s attorneys have extensive expertise and experience representing investors in securities litigation, and have recovered hundreds of millions of dollars for aggrieved shareholders. Attorney advertising. Prior results do not guarantee similar outcomes.

CONTACT:

Levi & Korsinsky, LLP
Joseph E. Levi, Esq.
30 Broad Street – 24th Floor
New York, NY 10004
Tel: (212) 363-7500
Toll Free: (877) 363-5972
Fax: (212) 363-7171
www.zlk.com

SOURCE: Levi & Korsinsky, LLP

ReleaseID: 474085

Theralase Increases Revenue 14% for 2Q2017 Financial Statements

TORONTO, ON / ACCESSWIRE / August 29, 2017 / Theralase Technologies Inc. (“Theralase®” or the “Company”) (TSXV: TLT) (OTCQX: TLTFF), a leading biotech company focused on the commercialization of medical devices to eliminate pain and the development of Photo Dynamic Compounds (“PDCs”) to destroy cancer, announced today that for the six-month period ended June 30, 2017, total revenue increased to $1,016,734 from $893,138 for the same period in 2016, a 14% increase.

In Canada, revenue increased 55% to $769,840 from $497,378. In the US, revenue decreased 33% to $211,453 from $316,756 and international revenue decreased 55% to $35,441 from $79,004. The increase in Canadian revenue in 2017 and the corresponding decrease in US and international revenue is attributable to the Company systematically building its sales and marketing teams in the Canadian market, the learning curves associated with training and developing a new sales force in the US and the ramp-up strategy of successfully commercializing the TLC-2000 therapeutic laser system to a recurring revenue model.

Cost of sales for the six-month period ended June 30, 2017 was $394,068 (39% of revenue) resulting in a gross margin of $622,666 or 61% of revenue, compared to a cost of sales of $302,879 (34% of revenue) in 2016, resulting in a gross margin of $590,259 or 66% of revenue. Cost of sales is represented by the following costs: raw materials, subcontracting, direct and indirect labour and the applicable share of manufacturing overhead.

Cost of sales increased primarily due to the retention of external engineering teams in order to optimize the TLC-2000 therapeutic laser system software, firmware and hardware to support the Company mandate of successfully commercializing the TLC-2000 for a recurring revenue model in 2018.

Sales and marketing expenses for the six-month period ended June 30, 2017 were $898,258 representing 88% of sales, compared with $665,727 or 75% of sales in 2016.

The increase is primarily due to increased spending on sales and marketing personnel, which are intended to augment sales of the TLC-2000 in future financial quarters. Selling expenses are expected to continue to increase in the future as the Company expands sales and marketing operations in Canada, the US and international markets. On-going investment in: sales personnel, marketing events and advertising are required expenses to generate and increase revenues in subsequent financial quarters.

Administrative expenses for the six-month period ended June 30, 2017 were $1,522,916 representing a 5% increase from $1,452,732 in 2016.

Increases in administrative expenses are attributed to the following:

Insurance expenses increased 28% due to increased product liability coverage
Professional fees increased by 111%, as a result of increased patent related fees for the Photo Dynamic Therapy (“PDT”) division.
Administrative salaries increased by 16%, as a result of hiring additional clinical and educational staff.

Gross research and development expenses totaled $1,433,968 for the six-month period ended June 30, 2017 compared to $925,504 in 2016 (55% increase). The increase in research and development expenses is a direct result of the ongoing investment in a Phase Ib clinical trial for Non-Muscle Invasive Bladder Cancer (“NMIBC”). Research and development expenses represented 37% of the Company’s operating expenses for the year and represent direct investment into the research and development expenses of the TLC-3000 anti-cancer technology.

The net loss for the six-month period ended June 30, 2017 was $3,238,023 which included $338,825 of net non-cash expenses (i.e.: amortization, stock-based compensation expense, foreign exchange gain/loss and lease inducements), with the PDT division represented $1,512,622 of this loss (47%). This compared to a net loss for the same period in 2016 of $2,456,417, which included $422,726 of net non-cash expenses, where the PDT division represented 1,669,988 of this loss (68%).

The increase in net loss is primarily due to increased investment in research and development of the TLC-3200 Medical Laser and TLC-3400 Dosimetry Fibre Optic Cage related to the support of a Phase Ib NMIBC clinical study and engineering, sales, marketing and administrative personnel initiatives for the optimization and commercialization of the TLC-2000 therapeutic laser system.

The PDT division is focused on successfully completing a Phase Ib clinical trial for patients afflicted with NMIBC, utilizing its novel next generation light-activated, anti-cancer drug, TLD-1433.

The TLT division is focused on successfully commercializing the next generation TLC-2000 therapeutic medical laser system and its associated recurring revenue model in 2018.

About Theralase Technologies Inc.

Theralase Technologies Inc. (“Theralase®” or the “Company”) (TSXV: TLT) (OTCQX: TLTFF) in its Therapeutic Laser Technology (“TLT”) Division designs, manufactures, markets and distributes patented super-pulsed laser technology indicated for the treatment of chronic knee pain and in off-label use the elimination of pain, reduction of inflammation and dramatic acceleration of tissue healing for numerous nerve, muscle, tendon, ligament, joint and wound conditions. Theralase’s Photo Dynamic Therapy (“PDT”) Division researches and develops specially designed molecules called Photo Dynamic Compounds (“PDCs”), which are able to localize to cancer cells and then when laser light activated, effectively destroy them.

Additional information is available at www.theralase.com and www.sedar.com.

This news release contains “forward-looking statements” which reflect the current expectations of management of the Corporation’s future growth, results of operations, performance and business prospects and opportunities. Such statements include, but are not limited to, statements regarding the proposed use of proceeds. Wherever possible, words such as “may,” “would,” “could,” “should,” “will,” “anticipate,” “believe,” “plan,” “expect,” “intend,” “estimate,” “potential for” and similar expressions have been used to identify these forward-looking statements. These statements reflect management’s current beliefs with respect to future events and are based on information currently available to management. Forward-looking statements involve significant risks, uncertainties and assumptions. Many factors could cause the Corporation’s actual results, performance or achievements to be materially different from any future results, performance or achievements that may be expressed or implied by such forward-looking statements; including, without limitation, those listed in the filings made by the Corporation with the Canadian securities regulatory authorities (which may be viewed at www.sedar.com). Should one or more of these risks or uncertainties materialize, or should assumptions underlying the forward looking statements prove incorrect, actual results, performance or achievements may vary materially from those expressed or implied by the forward-looking statements contained in this news release. These factors should be considered carefully and prospective investors should not place undue reliance on the forward-looking statements. Although the forward-looking statements contained in the news release are based upon what management currently believes to be reasonable assumptions, the Corporation cannot assure prospective investors that actual results, performance or achievements will be consistent with these forward-looking statements. The Corporation disclaims any intention or obligation to revise forward-looking statements whether as a result of new information, future developments or otherwise except as required by law. All forward-looking statements are expressly qualified in their entirety by this cautionary statement.

Neither TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchanges) accepts responsibility for the adequacy or accuracy of this release.

For More Information:

Roger Dumoulin-White
President & CEO
1.866.THE.LASE (843-5273) ext. 225
416.699.LASE (5273) ext. 225
rwhite@theralase.com
www.theralase.com

SOURCE: Theralase Technologies Inc.

ReleaseID: 474086

FTI INVESTOR ALERT: The Law Offices of Vincent Wong Notifies Investors of Commencement of a Class Action Involving TechnipFMC plc and a Lead Plaintiff Deadline of October 2, 2017

NEW YORK, NY / ACCESSWIRE / August 29, 2017 / The Law Offices of Vincent Wong announce that a class action lawsuit has been commenced in the United States District Court for the Southern District of Texas, Houston Division on behalf of investors who purchased TechnipFMC plc (”TechnipFMC”) (NYSE: FTI) securities between April 27, 2017 and July 24, 2017.

Click here to learn about the case: http://www.wongesq.com/pslra-sb/technipfmc-plc?wire=1. There is no cost or obligation to you.

According to the complaint, throughout the Class Period, the Company issued materially false and misleading statements and/or failed to disclose that: (i) TechnipFMC had a material weakness in its internal control over rates used in the calculations of the foreign currency effects on certain of its engineering and construction projects; (ii) accordingly, the Company lacked effective internal controls over financial reporting; and (iii) as a result of the foregoing, TechnipFMCs public statements were materially false and misleading at all relevant times.

If you suffered a loss in TechnipFMC you have until October 2, 2017 to request that the Court appoint you as lead plaintiff. Your ability to share in any recovery doesn’t require that you serve as a lead plaintiff. To obtain additional information, contact Vincent Wong, Esq. either via email vw@wongesq.com, by telephone at 212.425.1140, or visit http://www.wongesq.com/pslra-sb/technipfmc-plc?wire=1.

Vincent Wong, Esq. is an experienced attorney that has represented investors in securities litigations involving financial fraud and violations of shareholder rights. Attorney advertising. Prior results do not guarantee similar outcomes.

CONTACT:

Vincent Wong, Esq.
39 East Broadway
Suite 304
New York, NY 10002
Tel. 212.425.1140
Fax. 866.699.3880
E-Mail: vw@wongesq.com

SOURCE: The Law Offices of Vincent Wong

ReleaseID: 474080

Patriot Scientific Corporation Files Annual Report

CARLSBAD, CA / ACCESSWIRE / August 29, 2017 / Patriot Scientific Corporation (OTC PINK: PTSC) today announced it has filed its Report on Form 10-K with the U.S. Securities and Exchange Commission for the annual period ended May 31, 2017. The Report can be found on the SEC’s website at https://www.sec.gov/edgar/searchedgar/companysearch.html.

About Patriot Scientific Corporation

Headquartered in Carlsbad, California, Patriot Scientific Corporation is the co-owner of the Moore Microprocessor Patent Portfolio™. For more information on PTSC, visit www.ptsc.com.

About the MMP Portfolio™

The MMP Portfolio includes US patents as well as their European and Japanese counterparts, which cover techniques that enable higher performance and lower cost designs essential to consumer and commercial digital systems ranging from PCs, cell phones and portable music players to communications infrastructure, medical equipment and automobiles.

Contact:

Patriot Scientific Corp
760-795-8517

SOURCE: Patriot Scientific Corporation

ReleaseID: 474087

The Klein Law Firm Notifies Investors of Commencement of a Class Action Filed on Behalf of Teva Pharmaceutical Industries Ltd. Shareholders and a Lead Plaintiff Deadline of October 23, 2017 (TEVA)

NEW YORK, NY / ACCESSWIRE / August 29, 2017 / The Klein Law Firm announces that a class action complaint has been filed on behalf of shareholders of Teva Pharmaceutical Industries Ltd. (NYSE: TEVA) who purchased American Depositary Shares between November 15, 2016 and
August 2, 2017. The action, which was filed in the United States District Court for the Eastern District of Pennsylvania, alleges that the Company violated federal securities laws.

In particular, the complaint alleges that throughout the class period Defendants issued materially false and/or misleading statements and/or failed to disclose adverse information concerning the Company’s business and outlook. In particular, it is alleged that Teva failed to disclose and/or omitted the true negative impact of the acquisition and integration of Actavis Generics on the Company’s financial results and business prospects.

Shareholders have until October 23, 2017 to petition the court for lead plaintiff status. Your ability to share in any recovery does not require that you serve as lead plaintiff. You may choose to be an absent class member.

If you suffered a loss during the class period and wish to obtain additional information, please contact Joseph Klein, Esq. by telephone at 212-616-4899 or visit http://www.kleinstocklaw.com/pslra-sbm/teva-pharmaceutical-industries-ltd?wire=1.

Joseph Klein, Esq. is an experienced attorney and has also practiced as a Certified Public Accountant. Mr. Klein represents investors and participates in securities litigations involving financial fraud throughout the nation. Attorney advertising. Prior results do not guarantee similar outcomes.

CONTACT:

Joseph Klein, Esq.
Empire State Building
350 Fifth Avenue
59th Floor
New York, NY 10118
Telephone: (212) 616-4899
Fax: (347) 558-9665
www.kleinstocklaw.com

SOURCE: The Klein Law Firm

ReleaseID: 474081

Duluth Plastic Surgeon & Facelift Rhinoplasty Liposuction Surgery Site Launched

The acclaimed Atlantic Center for Plastic & Cosmetic Surgery, with consultations available at 770 418-1234, announced the launch of a new website showcasing the natural results its face, breast and body plastic surgery procedures deliver patients throughout the Duluth and Atlanta area.

Duluth Plastic Surgeon & Facelift Rhinoplasty Liposuction Surgery Site Launched

Duluth, United States – August 29, 2017 /PressCable/

The popular Atlantic Center for Plastic & Cosmetic Surgery has announced the launch of a new website showcasing the coveted plastic surgery procedures and natural results delivered by its board certified surgeon Dr. R. Morgan Davoudi for patients in the Atlanta, Georgia area.

More information is available at http://www.myatlantaplasticsurgeon.com/

The Atlantic Center for Plastic & Cosmetic Surgery is an acclaimed plastic surgery practice based in Duluth, Georgia, with more than a decade of experience helping patients across the Atlanta area look and feel their best with a range of quality surgical and non-surgical procedures for all areas of the face and body.

The popular cosmetic surgery practice has now announced the launch of a new website with detailed information and extensive before & after photo galleries showcasing the natural, soft and flawless results it delivers patients looking for the best breast augmentation, lift or reduction and liposuction, tummy tuck, facelift, rhinoplasty or full mommy makeover procedures.

Its renowned range of plastic surgery procedures, laser treatments and Botox, Restylane or Juvederm med spa services are delivered by the experienced, talented and double board certified plastic surgeon Dr. R. Morgan Davoudi and a team of well-trained professionals committed to ensuring the most comfortable, personable and dedicated care before and after the surgery. For more details at http://www.myatlantaplasticsurgeon.com/html/breastaugmentationatlanta.php

Consultations and appointments with Dr. R. Morgan Davoudi and the Atlantic Center for Plastic & Cosmetic Surgery or more information on its range of surgical and non-surgical cosmetic procedures are available at 770 418-1234 or through the new website at the link provided above along with multiple patient testimonials, current discount specials and details on its state of the art facilities conveniently located at 3855 Pleasant Hill Rd. Suite 300, Duluth, Georgia.

The Atlantic Center for Plastic & Cosmetic Surgery explains that “Dr. Davoudi has dedicated his life to the art of cosmetic surgery and is entirely focused on helping each patient enhance their beauty and confidence in the most comfortable environment possible. We understand that choosing a plastic surgeon is an extremely important decision and it’s critical that both the surgeon and supporting staff are talented and personable. That’s what they’ll find with us.” Learn more at http://www.myatlantaplasticsurgeon.com/html/liposuctionatlanta.php

Contact Info:
Name: R. Morgan Davoudi, M.D
Organization: Atlantic Center for Plastic and Cosmetic Surgery
Address: 3855 Pleasant Hill Rd Suite 300, Duluth, GA 30096, United States
Phone: +1-770-418-1234

For more information, please visit http://www.myatlantaplasticsurgeon.com

Source: PressCable

Release ID: 233898

ABCO EQUITY ALERT: The Law Offices of Vincent Wong Notifies Investors of a Class Action Involving The Advisory Board Company and a Lead Plaintiff Deadline of October 2, 2017

NEW YORK, NY / ACCESSWIRE / August 29, 2017 / The Law Offices of Vincent Wong announce that a class action lawsuit has been commenced in the United States District Court for the Southern District of New York on behalf of investors who purchased The Advisory Board Company (“Advisory Board”) (NASDAQ: ABCO) securities between January 21, 2015 and February 23, 2016.

Click here to learn about the case: http://www.wongesq.com/pslra-sb/the-advisory-board-company?wire=1. There is no cost or obligation to you.

According to the complaint, throughout the Class Period, the Company issued materially false and misleading statements and/or failed to disclose that: (1) there were severe integration problems associated with Advisory Board’s acquisition of Royall & Company; and (2) as a consequence, defendants had no basis to increase the revenue guidance for Royall during the Class Period. On January 9, 2015, Advisory Board completed its acquisition of Royall & Company. Then on February 23, 2016, Advisory Board announced a net loss of $101.8 million for the quarter ended December 31, 2015, primarily attributable to an impairment charge of $95.7 million (and later increased to $99.1 million) to Royall’s goodwill. Following this news, shares of Advisory Board fell 27% to close at $26.50 per share on February 24, 2016.

If you suffered a loss in Advisory Board you have until October 2, 2017 to request that the Court appoint you as lead plaintiff. Your ability to share in any recovery doesn’t require that you serve as a lead plaintiff. To obtain additional information, contact Vincent Wong, Esq. either via email vw@wongesq.com, by telephone at 212.425.1140, or visit http://www.wongesq.com/pslra-sb/the-advisory-board-company?wire=1.

Vincent Wong, Esq. is an experienced attorney that has represented investors in securities litigations involving financial fraud and violations of shareholder rights. Attorney advertising. Prior results do not guarantee similar outcomes.

CONTACT:

Vincent Wong, Esq.
39 East Broadway
Suite 304
New York, NY 10002
Tel. 212.425.1140
Fax. 866.699.3880
E-Mail: vw@wongesq.com

SOURCE: The Law Offices of Vincent Wong

ReleaseID: 474077

INVESTOR ALERT: Levi & Korsinsky, LLP Notifies Shareholders of Applied Optoelectronics, Inc. of a Class Action Lawsuit and a Lead Plaintiff Deadline of October 4, 2017 – AAOI

NEW YORK, NY / ACCESSWIRE / August 29, 2017 / The following statement is being issued by Levi & Korsinsky, LLP:

To: All persons or entities who purchased or otherwise acquired securities of Applied Optoelectronics, Inc. (“Applied Optoelectronics”) (NASDAQ: AAOI) between July 13, 2017 and August 3, 2017. You are hereby notified that a securities class action lawsuit has been commenced in the United States District Court for the Southern District of Texas. To get more information go to: http://www.zlk.com/pslra-sba/applied-optoelectronics-inc?wire=1 or contact Joseph E. Levi, Esq. either via email at jlevi@levikorsinsky.com or by telephone at (212) 363-7500, toll-free: (877) 363-5972. There is no cost or obligation to you.

The complaint alleges that throughout the class period Defendants issued materially false and/or misleading statements and/or failed to disclose that: (1) a major customer was reducing its purchases of the Company’s 40G receivers; (2) the loss of this major customer’s business would have a severe negative impact on the Company’s financial performance; and (3) as a result, the Company’s public statements were materially false and misleading at all relevant times.

If you suffered a loss in Applied Optoelectronics you have until October 4, 2017 to request that the Court appoint you as lead plaintiff. Your ability to share in any recovery doesn’t require that you serve as a lead plaintiff.

Levi & Korsinsky is a national firm with offices in New York, California, Connecticut, and Washington D.C. The firm’s attorneys have extensive expertise and experience representing investors in securities litigation, and have recovered hundreds of millions of dollars for aggrieved shareholders. Attorney advertising. Prior results do not guarantee similar outcomes.

CONTACT:

Levi & Korsinsky, LLP
Joseph E. Levi, Esq.
30 Broad Street – 24th Floor
New York, NY 10004
Tel: (212) 363-7500
Toll Free: (877) 363-5972
Fax: (212) 363-7171
www.zlk.com

SOURCE: Levi & Korsinsky, LLP

ReleaseID: 474072