[Posted 02/09/2017] AUDIENCE: Consumer, Emergency Medicine ISSUE: Kingsway Trading Inc. is recalling its 1.06 oz (30g) bottles of “Well Balance Xanthium Siler Combo (Bi Yan Pian)” Batch No. 130401 Batch No. 150201 because they contain the presence of undeclared Ephedra Herba (ma huang), an FDA banned item. Dietary supplements containing ephedrine alkaloids pose a risk…
Chlorhexidine Gluconate: Drug Safety Communication
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Halo One Thin-Walled Guiding Sheath by Bard Peripheral Vascular Inc.: Class I Recall
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Certain Homeopathic Teething Products: FDA Warning- Confirmed Elevated Levels of Belladonna
[Posted 01/27/2017] AUDIENCE: Consumer ISSUE: FDA announced that its laboratory analysis found inconsistent amounts of belladonna, a toxic substance, in certain homeopathic teething tablets, sometimes far exceeding the amount claimed on the label. The agency is warning consumers that homeopathic teething tablets containing belladonna pose an unnecessary risk to infants and children and urges consumers…
NucliSENS easyMAG Magnetic Silica and NucliSENS Magnetic Extraction Reagents by bioMerieux: Recall
[Posted 01/27/2017] AUDIENCE: Laboratory, Patient, Pathology ISSUE: This is a continuation of bioMerieux’s previous recall for NucliSENS easyMAG Magnetic Silica. The firm has identified additional affected product lots, and an additional product, the NucliSENS Magnetic Extraction Reagents, which have been determined to be in scope of the previous recall. bioMerieux is recalling the NucliSENS reagents…
NucliSENS easyMAG Magnetic Silica and NucliSENS Magnetic Extraction Reagents by bioMerieux: Class I Recall
[Posted 01/27/2017] AUDIENCE: Laboratory, Patient, Pathology ISSUE: This is a continuation of bioMerieux’s previous recall for NucliSENS easyMAG Magnetic Silica. The firm has identified additional affected product lots, and an additional product, the NucliSENS Magnetic Extraction Reagents, which have been determined to be in scope of the previous recall. bioMerieux is recalling the NucliSENS reagents…
Vancomycin Hydrochloride for Injection, USP by Hospira: Recall
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ED-3490TK Video Duodenoscope by Pentax: FDA Safety Communication – UPDATE
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Lifepak 1000 Defibrillators by Physio-Control: Voluntary Field Action
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Duodenoscopes by Fujifilm Medical Systems: Safety Communication
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