Medtronic Recalls Duet EDMS Catheter for Disconnection Issue
Medtronic Neurosurgery is recalling the Duet EDMS catheter tubing due to a potential for catheter disconnection.
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Search Results for: recall
Philips Recalls BrightView Imaging Systems
Philips has recalled its BrightView SPECT imaging systems for a potential component failure that would cause parts to fall on the patient.
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GS1 US Publishes Guidelines for Advanced 2D Barcodes
GS1 US released new guidelines for transitioning to more-advanced 2D barcodes on product packaging in the U.S. healthcare sector.
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Philips Stops Selling Respiratory Products in the U.S.
Philips announced that it would stop selling CPAP or BiPAP sleep therapy devices and other respiratory care devices in the U.S.
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GAO to Investigate FDA’s Medical Device Oversight
The Government Accountability Office (GAO) is launching an investigation into the U.S. FDA’s potentially ineffective policies for recalling medical devices, prompted by concerns raised by Senators Durbin and Blumenthal regarding the slow response to recalls of Philips Respironics CPAPs, BiPAPs, and mechanical ventilators.
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