FDA Raises Concern vs Other Stryker’s Medical Devices, Aside From Artificial Hips

In addition to Stryker’s recalled hip replacement devices, Rejuvenate and ABG II, the Food and Drug Administration (FDA) has warned the public about the company’s two medical devices named Neptune 1 Silver and Neptune 2 Ultra Waste, according to media reports. These two medical suctions are used to collect and remove liquid surgical wastes and smoke during procedures that use laser or other electrical devices. The FDA warned that if these devices are incorrectly used, it may cause hemorrhage or cause damage to muscle, soft tissues or vital organs, which may lead to serious health complications. Many recipients across the United States have filed lawsuits against Stryker for injuries they have suffered, and the number of lawsuits is expected to increase as more device failures are reported.

Read more: FDA Warns Against Other Stryker Medical Devices in Addition to Hip Replacements

The Rottenstein Law Group Advises Caution Before Calling Stryker Hip Replacement Recall “Care Line”

The Rottenstein Law Group cautions recipients of two recalled Stryker-manufactured replacement hip devices to speak to a lawyer before calling Stryker’s “care line,” because any information provided to Stryker could be used by Stryker to avoid responsibility for the harms caused by the device.

New York, New York (PRWEB) January 08, 2013

The Rottenstein Law Group urges recipients of the recalled Stryker Rejuvenate and ABG II hip replacement devices to think twice before calling the Stryker hip replacement recall “care line.”

Stryker, maker of the Rejuvenate Modular and ABG II hip replacement systems recalled in July 2012, has announced it teamed up with third-party claims company Broadspire to address and manage medical claims and out-of-pocket costs against the company.

Read full story at PRWeb:  The Rottenstein Law Group Advises Caution Before Calling Stryker Hip Replacement Recall “Care Line”