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. 2,332 recalls have been distributed to Vermont in the last 12 months.
Showing 24961–24980 of 47,027 recalls
Recalled Item: Nirvanio Maeng Da Kratom all packages Recalled by Nutrizone LLC Due to...
The Issue: Dietary supplements have the potential to be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pain Out Green Malay Kratom all packages Recalled by Nutrizone LLC Due to...
The Issue: Dietary supplements have the potential to be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cali Thai Kratom all packages Recalled by Nutrizone LLC Due to Potential...
The Issue: Dietary supplements have the potential to be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pain Out Thai Kratom all packages Recalled by Nutrizone LLC Due to Potential...
The Issue: Dietary supplements have the potential to be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cali Maeng Da Kratom all packages Recalled by Nutrizone LLC Due to Potential...
The Issue: Dietary supplements have the potential to be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: C2 CryoBalloon Focal Catheter Recalled by PENTAX of America Inc Due to The...
The Issue: The catheter alignment arrow printed onto the strain relief is not aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR Surgical Suite Option Product The MR Surgical Option when Recalled by GE...
The Issue: There is a potential safety issue with the table transfer release of the MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coronary Sinus (CS) Uni-Directional Diagnostic Electrophysiology (EP)...
The Issue: Thrombogenicity test results demonstrated that both the test devices (SSS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental System Proximal Femoral Component 38mm Offset Recalled by...
The Issue: There is a potential for debris in the hole on the superior lateral aspect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 24-HOUR Oral Care q2 Kit with Ballard* Technology Recalled by Akorn, Inc....
The Issue: Subpotent Drug: Product crystallization with accompanying low out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zhong Hua Jiu (menthol 1%) Patch Recalled by United Pacific Co Ltd Due to...
The Issue: CGMP Deviations: the product was produced with substandard GMP manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 24-HOUR Oral Care q4 Kit with Ballard* Technology Recalled by Akorn, Inc....
The Issue: Subpotent Drug: Product crystallization with accompanying low out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chlorhexidine Gluconate Oral Rinse Recalled by Akorn, Inc. Due to Subpotent...
The Issue: Subpotent Drug: Product crystallization with accompanying low out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chocolate Sea Salt Probiotic Granola Recalled by purely elizabeth. Due to...
The Issue: Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...
The Issue: The dose calculation accuracy may in some situations be less than expected....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Acute Care System (lACS) Monitoring Solution Recalled by Draegar...
The Issue: Software anomaly resulting in the loss of patient settings and stored...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.