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. 2,244 recalls have been distributed to Vermont in the last 12 months.
Showing 43381–43400 of 47,027 recalls
Recalled Item: Olympus Endoscopic Flushing Pump Recalled by Olympus America Inc. Due to...
The Issue: There is a possibility that the pump head was not shipped in the locked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERIS Fine Traction Device Recalled by Steris Corporation Due to A bearing...
The Issue: A bearing used in the assembly of the Fine Traction Device did not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enablex (darifenacin) Extended Release Tablet Recalled by Warner Chilcott US...
The Issue: Failed Impurities/Degradation Specifications: unspecified degradation product
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BASE Recalled by SpineFrontier, Inc. Due to The S-LIFT Instrument Case...
The Issue: The S-LIFT Instrument Case contained a bracket with peeling nylon coating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Code Alert Advanced 4-Way Care Solution Recalled by RF Technologies, Inc....
The Issue: RF Technologies, Inc. has initiated a recall involving CA520 Code Alert...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: West-ward Belladonna Alkaloids with Phenobarbital Tablets Recalled by...
The Issue: Presence of Foreign Substance: Belladonna Alkaloids with Phenobarbital...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: West-ward Belladonna Alkaloids with Phenobarbital Tablets Recalled by...
The Issue: Cross contamination with other products: Belladonna Alkaloids with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Solbar Q Soy Protein Isolates. Item No. / Item Description: Recalled by Chs...
The Issue: Certain Soy-based products produced at the Ashdod Israel production facility...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Contex - Textured Soy Protein Concentrates Item No. / Item Recalled by Chs...
The Issue: Certain Soy-based products produced at the Ashdod Israel production facility...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Solcon Soy Protein Concentrates. Item No. / Item Description: 12110 Recalled...
The Issue: Certain Soy-based products produced at the Ashdod Israel production facility...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Solcon S Functional Soy Protein Concentrates. Item No. / Item Recalled by...
The Issue: Certain Soy-based products produced at the Ashdod Israel production facility...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Superstand stand-up wheelchair HPS-2 A standup wheelchair is a device...
The Issue: Power Superstand Standing Wheel chair, flex shaft (the flexible wand which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with Unitized BactiSeal...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with Siphonguard Recalled by...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve only with SiphonGuard...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve with Catheter and Recalled by...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Certas Programmable Valve In Line Valve Only Product Code: Recalled...
The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.