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. 2,356 recalls have been distributed to Vermont in the last 12 months.
Showing 20441–20460 of 47,027 recalls
Recalled Item: PROBAR MEAL Wholeberry Blast Recalled by Probar LLC Due to Undeclared Milk
The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is Recalled by...
The Issue: code 7-102 Liquid Sensor Error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gablofen (baclofen injection) Recalled by Piramal Critical Care, Inc. Due to...
The Issue: Failed Impurities/Degradation Specification -This recall is being initiated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD FACS Sample Prep Assistant (SPA) II - Product Usage: Recalled by Becton,...
The Issue: The recalling firm confirmed that BD FACS Sample Prep Assistant (SPA) II and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACS Sample Prep Assistant (SPA) III - Product Usage: Recalled by Becton,...
The Issue: The recalling firm confirmed that SPA II and III users may encounter probes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACS Sample Prep Assistant (SPA) II Upgrade - Product Recalled by Becton,...
The Issue: The recalling firm confirmed that SPA II and III users may encounter probes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GRIPPER Needles sold individually. Labeled as the following item...
The Issue: Potential for certain GRIPPER Needles to contain an occluded or blocked needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GRIPPER Needles sold as part of PORT-A-CATH II SINGLE LUMEN Recalled by...
The Issue: Potential for certain GRIPPER Needles to contain an occluded or blocked needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TransWarmer Warming Infant Transport Mattress Recalled by CooperSurgical,...
The Issue: The firm updated the IFU in April 2019 to clarify that use of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho Clinical Diagnostics Due to Potential...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho Clinical Diagnostics Due to Potential...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 32 Recalled by Ortho Clinical...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250AT Chemistry System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 350 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho Clinical Diagnostics Due to...
The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.