Integra LifeSciences Corporation, Plainsboro, New Jersey, has initiated a worldwide recall of the NeuroBalloon Catheter. There were a total of 1,924 units distributed, 258 in the United States of America 1,586 in the European Union and 80 in countries.

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Integra Issues URGENT Worldwide Recall of NeuroBalloonTM Catheter

Device computer may shut down without an alarm, which can lead to serious injuries or death.

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Abiomed AB5000 Circulatory Support System: Class I Recall

Reports of serious injuries and at least one death have been associated with increased Intraperitoneal Volume (IIPV), also known as overfill of the abdominal cavity.

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Baxter HomeChoice and HomeChoice PRO Automated Peritoneal Dialysis Systems: Class I Recall

Consumers warned not to use ear candles because they can cause serious injuries, even when used according to the manufacturer’s directions.

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Ear Candles: Risk of Serious Injuries