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.
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Hospira 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.
Read MoreFDA Announces Plan to Speed Access to New Device Technologies
Dec 7, 2012 | Government Regulations, Recalls | 0 |
The FDA announces that it is part of the first public-private partnership to promote medical device regulatory science with a focus on speeding the development, assessment, and review of new medical devices.
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