Product Recalls in Connecticut
Product recalls affecting Connecticut — including food, drugs, consumer products, medical devices, and vehicles distributed to Connecticut. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,054 recalls have been distributed to Connecticut in the last 12 months.
Showing 16881–16900 of 51,038 recalls
Recalled Item: BIOTRONIK ITREVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK ILIVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK Ilestro 7 DR-T Recalled by BIOTRONIK Inc Due to There is a...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK ITREVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK ILIVIA NEO 7 DR-T DF-1 ProMRI Recalled by BIOTRONIK Inc Due to...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK Ilestro 7 VR-T DX Recalled by BIOTRONIK Inc Due to There is a...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK Ilestro 7 VR-T Recalled by BIOTRONIK Inc Due to There is a...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOTRONIK INVENTRA 7 Recalled by BIOTRONIK Inc Due to There is a potential...
The Issue: There is a potential for premature battery depletion in Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VEGAN VITAMIN D3 Recalled by New Generation Wellness Inc. Due to Vitamin D3...
The Issue: Vitamin D3 stability sample analyzed and found to be less than 100% of label...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Live Better vegan vitamin d-3 by CVS Health Recalled by New Generation...
The Issue: Vitamin D3 stability sample analyzed and found to be less than 100% of label...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gabapentin Oral Solution Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications; out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADVIA 2120 DAA AUTOSAMPLER (SMN 10374454) - OUS Recalled by Siemens...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i (RoHS) with Single Aspirate Autosampler (SMN 11219529) - US...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i Single Aspirate (SMN 11314044) - US Recalled by Siemens...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i with Single Aspirate Autosampler (SMN 10488923) - US Recalled by...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120 with Single Aspirate Autosampler (SMN 10316162) - OUS Recalled by...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120 Dual Aspirate Autosampler (SMN 10313419) - US Recalled by Siemens...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i (RoHS) with Single Aspirate Autosampler (SMN 11219529) - OUS...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120 DAA AUTOSAMPLER (SMN 10374454) - US Recalled by Siemens...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120 with Single Aspirate Autosampler (SMN 10316162) - US Recalled by...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.