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Recent Posts in Medical Device Failure Category

GE Healthcare Vital Signs Device Recalled

The U.S. Food and Drug Administration announced earlier this month that it has notified healthcare professionals of a Class I recall of the GE Healthcare Vital Signs Hygroscopic Condenser Humidifier ...
Continue reading "GE Healthcare Vital Signs Device Recalled" »

Women Claim Transvaginal Mesh Had Painful Side Affects

A handful of women have become co-plaintiffs in a lawsuit against the makers of transvaginal mesh, reports say. The complaints were raised after doctors of each of the women used the devices during ...
Continue reading "Women Claim Transvaginal Mesh Had Painful Side Affects" »

Epilepsy Drugs May Harm Fetal Development

Medications that control epilepsy, such as Depakote, Depakene and Depakon may affect a fetus if used during pregnancy, the U.S. Food & Drug Administration reportedly said recently. From that ...
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Blood Chemistry Analyzer Recalled

The medical device company Beckman Coulter, Inc., issued a recall in May for their Synchron LX Ion Selective Electrolyte Flow Cell, which is classified by the FDA as a Class I recall by the U.S. Food ...
Continue reading "Blood Chemistry Analyzer Recalled" »

Hip Implant Class Action Lawsuit Filed by Australians

The oft-maligned DePuy hip implant device, which was recalled last summer, has been cited in a lawsuit by 20 Australians earlier this month. The suit claims the device, which is surgically implanted ...
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Aortic Balloon Catheter Pumps Recalled

Reports say a defective fan may become overheated and shut down the Maquet Datascope Intra-Aortic Balloon Catheter Pump without sounding any warning alarm, and ultimately injuring patients. Due to ...
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Hip Implant Lawsuits Filed

Some 80 patients in Wisconsin have filed suit against DePuy Orthopaedics, saying the now-recalled ASR hip implants have caused pain, swelling and nerve and muscle damage, reports say The device, which ...
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Bypass Device Recalled

A device used in delivering a lifesaving cardioplegia solution to coronary arteries during cardiopulmonary bypass has been recalled, with consultation with the U.S. Food and Drug Administration, ...
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