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We Represent Clients Injured By Dialysis Drugs Dialysis drugs GranuFlo and NaturaLyte were the subjects of a Class 1 recall by the FDA after research found they can cause serious problems including death. -
FDA Recalls Dialysis Drugs Granuflo And Naturalyte Milwaukee pharmaceutical lawyers warn about the FDA Recall of Fresenius Medical Care's dialysis drugs Granuflo and Naturalyte and their side effects. -
J & J Reports Profit Losses Tied to DePuy ACR Hip Recall Johnson & Johnson, maker of recently recalled ASR hip joints and the subject of multiple class action lawsuits, is recording higher than expected profit. -
Avandia Finalizes Heart Attack Risk Warning Label The FDA recently ordered drug giant GlaxoSmithKline to change the label and use of their diabetes drug, Avandia. -
Avandia Maker to Pay Over $3.4 Billion in Damages GlaxoSmithKline are currently expecting to have to pay $3.4 billion to settle class action lawsuits. -
Recalled A.S.R. Hip Replacements Not FDA Approved A loophole in FDA approval procedures has allowed artificial joint makers to put artificial joints on the market without FDA approval, trial or testing. -
Could Metal Hip Implants Have a Negative Impact? Re-operation and re-replacement of defective hips may not be the only hip replacement issue that implant patients are facing. -
Recall Of Avandia, Other Prescription Drugs, A Danger In WI Should the FDA be doing more to prevent potentially dangerous drugs from entering the market? Many believe that the answer is yes. -
Johnson & Johnson Faces Recalls, Citations & Plant Closures Johnson & Johnson is in more trouble over quality control issues. The pharmaceutical giant has faced multiple recalls due to possible dangerous contamination. -
Hip Replacement Recalls Affect Wisconsin Though recall news involving any drug or device can be upsetting, when the recall involves a hip joint the prospect is downright frightening. -
Wisconsin Affected by Massive Infusion Pump Recalls The FDA has recently announced a rash of recalls over medical devices. The latest, a serious class 1 recall, involves the Sigma Spectrum Infusion Pump. -
FDA Takes a Closer Look at Defibrillators Though defibrillators can and do save thousands of lives a year, the FDA is concerned that the steady stream of recalls indicates a serious problem.
News About Pharmaceutical Class Action Cases
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