Philips Issues Recall to Upgrade Product
In the Enforcement Report for the week of January 2, 2013, the FDA listed the Class II recall of the Extended Brilliance workspace (EBW) in order to update the system.
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Fisher & Paykel Healthcare Class I Recall Continues
The FDA notified health care professionals that the Fisher & Paykel Healthcare reusable breathing circuit, model 900MR068, was recalled due to pinholes in the tubes used in the reusable breathing circuit.
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A Map for Success
Mixing a business approach with a patient-centric focus, the team at Thomas Jefferson University Hospitals delivers innovative and effective solutions.
Read MoreFDA Issues Notification of Class I Recall of Portable Oxygen Cylinder Units
Praxair Inc issued a recall of the Grab ‘n Go Vantage portable oxygen cylinder unit because fires may occur inside the cylinder unit causing the wall of the unit to break and release oxygen.
Read MoreGE Continues its Class II Recall of the Advantage Workstation
The FDA Enforcement Report for the week of December 26, 2012 lists the ongoing GE Healthcare LLC recall of the Advantage workstation.
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