Class I Recall

Class I ResMed Ventilator Recall

WASHINGTON, D.C. — Not long ago, the U.S. Food and Drug Administration (FDA) determined that ResMed’s Stellat invasive and non-invasive ventilator recall initiated should be designated a Class I recall. [...]

Recalled GE Anesthesia Devices Labeled High-Risk by the FDA

WASHINGTON, D.C. — The website Med Tech Drive recently published information regarding the recall of General Electric Healthcare’s defective anesthesia systems that have been recalled by the company and the [...]

The Medtronic Catheter recall has affected over 100,000 units across the nation.

Medtronic Catheter Recall Issued Following Cardiac Complication Risks

A Class I Medtronic Catheter recall has been mandated by the U.S. Food and Drug Administration following a series of disturbing complaints about the 6 French Sherpa NX Active Guide [...]

Personal Injury Lawsuit: Class I Recall Issued for Puritan Bennett 980 Ventilators

Puritan Bennett 980 Ventilators Injury Lawsuits. Our firm is investigating potential lawsuits on behalf of patients who suffered injuries or death related to the Puritan Bennett 980 Ventilator System [...]

St. Jude Medical Recalls Defibrillator Leads Due to Damaged Insulation

On January 22, 2016, device maker St. Jude Medical announced that a voluntary global field safety action related for the company’s Optisure Dual Coil Defibrillation Leads has now been designated [...]

Class I Recall Issued for Brainlab Cranial IGS System

The U.S. Food and Drug Administration (FDA) has puts its most serious Class I label on a recall of Brainlab’s Image-Guided Surgery (IGS) System. According to an FDA recall notification, [...]

HeartWare to Recall Ventricular Assist System

HeartWare Issues Updates to Recall Information for Ventricular Assist System

Device maker HeartWare has issued updated information on the multiple recalls for its Ventricular Assist Device (HVAD). The recalls were the result of five different types of complaints from users [...]

Change in Packaging Caused Class I Recall of Peripheral Vascular Patch, Baxter Says

A change in packaging caused a Class I recall of Baxter’s Vascu-Guard peripheral patch. The recall, which was initiated on May 2, 2015, affects the following four models of the [...]

FDA Class I Recall for TigerPaw II Heart Device

On May 7, 2015, the U.S. Food and Drug Administration (FDA) announced the recall of the TigerPaw System II by Maquet Medical Systems. The TigerPaw II is an implantable left [...]

More than 12,000 GE MRI Systems Recalled Due to Potentially Life-Threatening Issue

A Class I recall has been issued for more than 12,000 MRI systems manufactured by General Electric, Modern Healthcare reports. The recall was issued because of a potentially life-threatening problem [...]

What Our Clients Say About Us

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when 911 happened i had a very bad experience with my health but now i am better, i decided to contact the law firm of Parker Waichman for assistance, they referred me to Benita Rollins regarding my case, she took charge ,very knowledgeable lady ,helped me with the case ,they are the best law firm to contact regarding any issue with any matter simply the best ever !! especially Benita Rollins, ho has helped me with my issue very Graithful for help from this lady.

Frank Dimeglio

2 years ago

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louie m

a month ago

Hi there my name is Nicole Delia and I highly recommend this law firm. I've been working with Jessie Salcedo she's the paralegal on my case. She's always kind and very professional on the phone. I look forward to working with them. There location is 6 Harbor Drive Port Washington New York, NY 11050

Nicole Delia

5 years ago

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