Archive for September, 2009

Medtronic Issues Class I Recall for Catheters, Pump Kits

Filed September 25th, 2009 meg

Minneapolis, Minnesota-based Medtronic has announced a Class I Recall of several catheter and pump kits.
Included in the recall are the INDURA 1P Intrathecal Catheter, the Intrathecal Catheter, the Sutureless Pump Connector Revision Kit, and the Intrathecal Catheter Pump Segment Revision Kit.
The current labeling for catheters and revision kits incorrectly states that SC catheters are intended […]

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New Jersey lawmakers wrongly swayed FDA decision on knee patch

Filed September 25th, 2009 joshua


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Institute of Medicine to look at device review process

Filed September 25th, 2009 joshua


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FDA issues alert on Philips Lifeline Personal Help Button due to choking hazard

Filed September 24th, 2009 joshua


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Surgeon’s Ties with Medtronic Raises Questions

Filed September 23rd, 2009 meg


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Heart doctor pressed by Senators on payments from device makers

Filed September 22nd, 2009 joshua


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External defibrillators recalled

Filed September 18th, 2009 joshua


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FDA Cites Evenflo for Shock Risk of Breast Pumps

Filed September 17th, 2009 meg


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Medtronic recalls catheters

Filed September 17th, 2009 joshua


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Improper sizes prompts recall of pediatric tracheal tubes

Filed September 15th, 2009 joshua


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