Bunnell 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.
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Valve 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.
Read MoreBunnell Inc Recalls Life Pulse High-Frequency Ventilator Patient Circuits
On December 12, 2012 Bunnell Inc voluntarily initiated a nationwide recall notification of Life Pulse high-frequency ventilator patient circuits.
Read MoreNotice of the Class I Recall of the Olympic Cool-Cap System
The FDA notified health care professionals of a Class I Recall of the Olympic cool-cap system from Natus Medical Inc.
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