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. 2,356 recalls have been distributed to Connecticut in the last 12 months.
Showing 47261–47280 of 51,038 recalls
Recalled Item: 1% Low Fat Cottage Cheese distributed under the following labels Recalled by...
The Issue: Possible presence of metal fragments.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cottage Cheese with Chive distributed under the following labels and...
The Issue: Possible presence of metal fragments.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 4% Cottage Cheese distributed under the following labels and sizes: Recalled...
The Issue: Possible presence of metal fragments.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Monaco RTP System Radiation Therapy Treatment Planning System. Radiation...
The Issue: Patient needs to be positioned as indicated by the treatment plan.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Folic Acid Injection Recalled by Fresenius Kabi USA, LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zolpidem Tartrate Tablets 5 mg Recalled by American Health Packaging Due to...
The Issue: Unit Dose Mispackaging: This recall event is due to a random undetected...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nimodipine Capsules 30 mg Recalled by Sun Pharmaceutical Industries Inc. Due...
The Issue: Crystallization; crystallized nimodipine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride and 5% Dextrose Injection Recalled by Baxter...
The Issue: Lack of Assurance of Sterilty: Specific lot numbers of these products have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by Baxter Healthcare Corp. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metronidazole Injection USP Recalled by Baxter Healthcare Corp. Due to Lack...
The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium and 0.9% Sodium Chloride Injection Recalled by Baxter...
The Issue: Lack of Assurance of Sterility: Specific lot numbers of these products have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Baxter Recalled by Baxter Healthcare Corp. Due to leaking pouches
The Issue: leaking pouches
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JaDera Recalled by Dolphin Intertrade Corporation Due to Undeclared Sibutramine
The Issue: Marketed without an Approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: XIYOUJI QINGZHI CAPSULE Recalled by Dolphin Intertrade Corporation Due to...
The Issue: Marketed without an Approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ondansetron Injection Recalled by Hospira, Inc. Due to Presence of...
The Issue: Presence of Particulate; lot being recalled as a precaution due to the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methotrexate Injection Recalled by Sandoz Incorporated Due to Presence of...
The Issue: Presence of Particulate Matter: Found during examination of retention samples.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dimension Vista(R) 500 and Dimension Vista(R) 1500 - Reloaded Vista Recalled...
The Issue: There is the potential for the vial volume of "in use" Vista calibrators,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.