recall

Abbott recalls infant formula

On Sept. 22, Abbott initiated a voluntary recall of certain Similac-brand powder infant formulas because of the possibility of a…

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…

Drugs and Devices Today

2/11/10 Recall of AEDs On February 3, Cardiac Science Corporation issued a recall for about 12,200 automated external defibrillators because…

Engage Introducer recalled

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

FDA News

On April 30, McNeil Consumer Healthcare, in consulation with the U.S. Food and Drug Administration, issued a voluntary recall of…

FDA recalls Alere diagnostic tests

On July 11, the U.S. Food and Drug Administration (FDA) announced the recall Alere Triage’s rapid diagnostic test system, which…

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…

NeoProfen recalled

Lundbeck Inc. has recalled two lots of NeoProfen (ibuprofen lysine) that failed to meet a visible particulate quality requirement. NeoProfen…

Test strip recall

LifeScan, Inc., has voluntarily recalled eight lots of OneTouch SureStep Test Strips. Lot numbers are at: http://www.fda.gov/Safety/Recalls/ucm202119.htm.

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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