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. 2,664 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,664 in last 12 months

Showing 601620 of 51,038 recalls

DrugNovember 26, 2025· Golden State Medical Supply Inc.

Recalled Item: Baclofen Tablets USP Recalled by Golden State Medical Supply Inc. Due to...

The Issue: Presence of Foreign Tablets/Capsules

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 26, 2025· SOMERSET THERAPEUTICS LLC

Recalled Item: Cisatracurium Besylate Injection USP Recalled by SOMERSET THERAPEUTICS LLC...

The Issue: Subpotent product:out of specification assay results observed during long...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 26, 2025· SOMERSET THERAPEUTICS LLC

Recalled Item: Cisatracurium Besylate Injection USP Recalled by SOMERSET THERAPEUTICS LLC...

The Issue: Subpotent product:out of specification assay results observed during long...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 26, 2025· SOMERSET THERAPEUTICS LLC

Recalled Item: Cisatracurium Besylate Injection USP Recalled by SOMERSET THERAPEUTICS LLC...

The Issue: Subpotent product:out of specification assay results observed during long...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 26, 2025· Winder Laboratories, LLC

Recalled Item: Morphine Sulfate Oral Solution 100 mg / 5 mL (20 mg* / mL) Recalled by...

The Issue: Correct Labeled Product Mispack-Size stated on carton label did not match...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Beckman Coulter, Inc.

Recalled Item: Beckman Coulter UniCel Dxl 600 Recalled by Beckman Coulter, Inc. Due to...

The Issue: Beckman Coulter has determined that, due to a potential communication issue,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Beckman Coulter, Inc.

Recalled Item: Beckman Coulter UniCel Dxl 800 Recalled by Beckman Coulter, Inc. Due to...

The Issue: Beckman Coulter has determined that, due to a potential communication issue,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Remote Diagnostic Technologies Ltd.

Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...

The Issue: Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2025· Ferndale Laboratories, Inc.

Recalled Item: Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive...

The Issue: Butyrate tube cracks during actuation, rendering product unusable.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugNovember 24, 2025· Breckenridge Pharmaceutical, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 24, 2025· Breckenridge Pharmaceutical, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 24, 2025· ICU Medical, Inc.

Recalled Item: LifeShield Drug Library Management (DLM) Recalled by ICU Medical, Inc. Due...

The Issue: For certain customers, the Change Summary review option ceases to operate as...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2025· Draeger, Inc.

Recalled Item: Draeger Vapor 2000. Unheated Recalled by Draeger, Inc. Due to A certain...

The Issue: A certain component of affected devices was not delivered within...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing