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Alaris Pump Module recall

CareFusion has recalled Alaris Pump Module, Models 8100 because of possible dysfunctions that could lead to pump stoppage. Read more.

Davol XenMatrix Surgical Graft recall

The U.S. Food and Drug Administration notified healthcare professionals that several lots of XenMatrix Surgical Graft have been recalled because…

Defibtech, LLC, recall

Defibtech, LLC, has recalled DBP-2800 Battery Packs used in the Lifeline AED and ReviveR AED (semi-automatic external defibrillators). Read more…

Engage Introducer recalled

On Aug. 13, the U.S. Food and Drug Administration (FDA) announced the recall of 6 French Engage Introducers manufactured between…

Hospira infusers recalled

On Sept. 10, the U.S. Food and Drug Administration announced the recall of the Hospira Symbiq One-Channel and Two-Channel Infusers…

I-Flow ON-Q Pump recall

I-Flow has recalled its ON-Q Pump with ONDEMAND Bolus Button because the button may not lock down. Read more.

MedWatch: Product recalls

Recent product recalls include B. Braun Infusomat Space Infusion System, CareFusion Alaris PC Unit, Model 8015, and Dukal Benzalkonium Chloride…

Metronidazole recall announced

The U.S. Food and Drug Administration (FDA) announced that Teva Pharmaceuticals, USA is voluntarily recalling Metronidazole Tablets USP, 250mg, lot…

Voluntary recall of metronidazole

Sagent Pharmaceuticals, Inc., has issued a voluntary recall of metronidazole injection, USP 500 mg/100 mL because of nonsterility found in…

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