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 1641–1660 of 27,157 recalls
Recalled Item: Dexcom G7 iOS Application Recalled by Dexcom, Inc. Due to A bug in the 2.7.0...
The Issue: A bug in the 2.7.0 version of the G7 iOS App can cause the app to enter a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL CultureSwab EZ Collection and Transport System Recalled by Copan...
The Issue: Swabs for specimen collection may be prone to breakage during product usage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChannelCheck Convenience Pack Recalled by Healthmark Industries Co., Inc....
The Issue: During endoscope surveillance monitoring, a user facility identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 8888160341 Recalled by Cardinal Health 200, LLC Due to Packaging...
The Issue: Packaging defect may compromise sterility of the product. Use of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pre-filled Water Syringe Recalled by Healthmark Industries Co., Inc. Due to...
The Issue: During endoscope surveillance monitoring, a user facility identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 8888160119 Recalled by Cardinal Health 200, LLC Due to Packaging...
The Issue: Packaging defect may compromise sterility of the product. Use of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 8888160325 Recalled by Cardinal Health 200, LLC Due to Packaging...
The Issue: Packaging defect may compromise sterility of the product. Use of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 8888160333 Recalled by Cardinal Health 200, LLC Due to Packaging...
The Issue: Packaging defect may compromise sterility of the product. Use of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 8888160648 Recalled by Cardinal Health 200, LLC Due to Packaging...
The Issue: Packaging defect may compromise sterility of the product. Use of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 8888160556 Recalled by Cardinal Health 200, LLC Due to Packaging...
The Issue: Packaging defect may compromise sterility of the product. Use of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeShield Drug Library Management (DLM) Recalled by ICU Medical, Inc. Due...
The Issue: Firm has identified Drug Library Management defects in the software: 1) DLM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Drill Stop Kit is the version of the Mini Recalled by Implant Direct...
The Issue: The Drill stop kit contains incorrect components.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth...
The Issue: Product may have an off color affecting perfomance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Manual Resuscitator with Medium Adult Mask Recalled by SunMed...
The Issue: Affected lots were manufactured with B/V Filter incorrectly attached to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GM Helix Acqua Implant Recalled by Straumann USA LLC Due to It is possible...
The Issue: It is possible that a package labelled as an 11.5 mm implant may contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GM Helix Acqua Implant Recalled by Straumann USA LLC Due to It is possible...
The Issue: It is possible that a package labelled as an 11.5 mm implant may contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sample probe sucks a sample dispensed into a tube or Recalled by Beckman...
The Issue: A manufacturing defect in the sample probe (S probe). The corners of the tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sample probe sucks a sample dispensed into a tube or Recalled by Beckman...
The Issue: Sample probes with defective probe tips, when used with clinical chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5008X HDF Hemodialysis Blood Tubing Set Recalled by Fresenius Medical Care...
The Issue: Potential of blood leak occurring between the lower port of the venous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...
The Issue: Due to the potential that some units within specific lots were damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.