GE 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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Paving Roads Less Taken
Driven to begin outreach in the 1980s, the Iowa Health team now finds its efforts ahead of the curve.
Read MoreBunnell Recalls Life Pulse High-Frequency Ventilator Patient Circuits
The FDA notified health care professionals and their provider organizations of the Class I Recall of the Bunnell life pulse high-frequency ventilator patient circuits.
Read MoreValve Leak Prompts Ventlab Manual Resuscitator Recall
The FDA sent a notice of a Class I Recall, initiated July 11, 2012, of the Ventlab Corp adult and pediatric disposable, manual resuscitators.
Read MoreHospira Pump Recall Continues
The FDA Enforcement Report for the week of December 19, 2012 lists the ongoing Class II Recall of the Plum A+ single channel infusion pumps with plug-and-play modules from Hospira Inc, Lake Forest, Ill.
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