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. 2,541 recalls have been distributed to Vermont in the last 12 months.
Showing 2541–2560 of 47,027 recalls
Recalled Item: Straight Inflow/Bifurcated Outflow Line Kit. Model Number: 902-00038....
The Issue: Potential crack in the female connector located on the Heat Exchanger in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:...
The Issue: Potential for early life x-ray tube failure for mobile x-ray system due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:...
The Issue: Potential for early life x-ray tube failure for mobile x-ray system due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guide Wire with Ruler Tube 3x800 mm DIA Recalled by Stryker GmbH Due to The...
The Issue: The metal ring at the end of the Guide Wire with Ruler Tube may detach from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guide Wire with Ruler Tube 3x1000 mm DIA Recalled by Stryker GmbH Due to The...
The Issue: The metal ring at the end of the Guide Wire with Ruler Tube may detach from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GALT Guidewire Guidewires are intended for use in Recalled by Galt Medical...
The Issue: Due to a potential open seal in the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B Braun Interventional Coaxial Dilator Recalled by Galt Medical Corporation...
The Issue: Due to a potential open seal in the sterile barrier packaging .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B Braun Interventional ELITE HV Hemostasis Valve Introducer System by Galt...
The Issue: Due to a potential open seal in the sterile barrier packaging .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intraocular Lens. enVista Envy IOL Recalled by Bausch & Lomb Surgical, Inc....
The Issue: In response to an increased number of reports of toxic anterior segment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Introducer Kit- Tearaway MicroSlide Recalled by Galt Medical Corporation Due...
The Issue: Due to a potential open seal in the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Introducer Needle These needles are used for the Recalled by Galt Medical...
The Issue: Due to a potential open seal in the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Introducer Kit- Coaxial Dilator Recalled by Galt Medical Corporation Due to...
The Issue: Due to a potential open seal in the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intraocular lens. enVista Monofocal IOL Recalled by Bausch & Lomb Surgical,...
The Issue: In response to an increased number of reports of toxic anterior segment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GALT Centeze Catheter DRC-002-06 The Centeze is intended Recalled by Galt...
The Issue: Due to a potential open seal in the sterile barrier packaging .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount Recalled by IHB OPERATIONS...
The Issue: The mounting hardware that is supplied with the 4FXS-60 monitor bracket does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cabot Creamery 8oz Extra Creamy Premium Butter Recalled by AGRI-MARK INC Due...
The Issue: Product contaminated with elevated levels of coliform.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Desert Farms Jalapeno Mustard. Caution to after opening. The Recalled by The...
The Issue: The product is in violation for not having an approved filed process and for...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Unisom Recalled by Chattem Inc Due to CGMP Deviations; detection of...
The Issue: CGMP Deviations; detection of Nitrosamine Drug Substance-Related Impurities...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: presence of Nitrosamine Drug Substance Related Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MTN OPS MULTI-V Men's Daily Multivitamin dietary supplement Recalled by MTN...
The Issue: Undeclared soy flour
Recommended Action: Do not consume. Return to store for a refund or discard.