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Defective Medical Devices

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Regulators Recall 465,000 Pacemakers After Finding Security Issues

The U.S. Food and Drug Administration (FDA) recently decided to recall 465,000 pacemakers due to security issues. Regulators feared that certain vulnerabilities with these...

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Investigation Finds FDA Delayed Warnings Against Power Morcellators

A new federal report has revealed that the Federal U.S. Food and Drug Administration (FDA) knew about the link between power morcellators and uterine...

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J & J Ordered to Pay $500 Million in Hip Implant Case

Earlier this month, a federal jury in Texas found Johnson & Johnson liable for $500 million in damages in a Pinnacle hip implant case...

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J & J Is Beginning to Settle Power Morcellator Cases

Manufacturer Johnson & Johnson has begun settling claims related to its power morcellator hysterectomy device which claimants say caused them harm by spreading undetected...

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Hip Implant Manufacturer is Subject of Court Cases

Zimmer Holdings Inc., maker of the Durom Cup hip implant, will soon have to fend off lawsuits over the medical device when two trials...

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Stryker Settlement Deadline Extended; Claims Are Being Filed

In November 2014, Stryker Corporation agreed to settle thousands of claims related to its metal-on-metal hip implant devices. Now, the deadline to register a...

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Australian Study Questions Effectiveness of DePuy Hip System

The following is an article that ran in the March 2010 Bioengineering Bulletin from the Department of Medical Engineering and Physics at the Royal...

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