Arterial Cannula Recall: Edwards Lifesciences Removes Arterial Cannula due to Risk of Wire Exposure
Edwards recalls arterial cannulae due to risk of wire exposure that may cause serious patient harm.
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Edwards recalls arterial cannulae due to risk of wire exposure that may cause serious patient harm.
Baxter is removing mobile lift components due to risk of false attachment, which may result in patient injury due to falls.
Medline Craniotomy Kits are procedure convenience kits. Kits containing the Codman Disposable Perforator are being corrected by Medline Industries.
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
MicroMyst Applicators are being recalled due to potential non-sterile product., but these devices may not have been properly sterilized.
Maquet is updating Servo Ventilator instructions due to a risk of inaccurate tidal volume delivery when the extended leak test is used.
Manual resuscitator recalled due to incorrect B/V filter assembly that could delay therapy. May cause hypoxia, hypercapnia, or death if used.
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
80.211.154.110