Product Recalls in Vermont
Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,712 recalls have been distributed to Vermont in the last 12 months.
Showing 40541–40560 of 47,027 recalls
Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...
The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicorette (nicotine polacrilex) Lozenges Mini Recalled by GlaxoSmithKline...
The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicorette Lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...
The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicorette Lozenge and NicoDerm CQ Recalled by GlaxoSmithKline Consumer...
The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...
The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...
The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...
The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicorette (nicotine polacrilex) Lozenges Mini Recalled by GlaxoSmithKline...
The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...
The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicotine polacrilex lozenge Recalled by GlaxoSmithKline Consumer Healthcare;...
The Issue: Failed Lozenge Specifications; Lozenges are overly thick, overly soft, and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atripla (efavirenz 600 mg/ emtricitabine 200 mg/ tenofovir disoproxil...
The Issue: Presence of Foreign Substance: Red Silicone Rubber Particulates are Present...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FreeStyle Flash Blood Glucose Monitors System. Meter made in China Recalled...
The Issue: Abbott Diabetes Care has identified through internal testing and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin I.V. Flush Syringe is available is pre-filled polypropylene syringes...
The Issue: The bar code that is printed on the Master Carton label does not correspond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Blood Glucose Monitors System. For in vitro diagnostic use...
The Issue: Abbott Diabetes Care has identified through internal testing and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Model numbers: M3535A Recalled...
The Issue: MRx may display a Red X in the Ready For Use (RFU) indicator during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical Systems,...
The Issue: A component of the MRx Processor Board may be susceptible to damage from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar Docking Station Recalled by Hospira Inc. Due to There are two...
The Issue: There are two situations that may occur when using the GemStar Docking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical...
The Issue: ECG trunk cable and connector block of the MRx could be susceptible to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur XP Immunoassay system Recalled by Siemens Healthcare...
The Issue: Instrument Cover Gas Spring failures. Over time, the gas spring may lose its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A with...
The Issue: When the HeartStart MRx.is used with the Q-CPR Meter in defibrillation mode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.