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. 2,623 recalls have been distributed to Connecticut in the last 12 months.
Showing 7361–7380 of 51,038 recalls
Recalled Item: CVS Health brand Lubricating Gel Drops (Polyethylene glycol 400 0.4%...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rugby brand Lubricating Tears Eye Drops (Dextran 70 0.1% Recalled by Kilitch...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leader brand Eye Irritation Relief (Polyvinyl alcohol 0.5% Recalled by...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leader brand Lubricant Eye Drops (Propylene glycol Eye Drops 0.6%) Recalled...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LUBRICANT EYE DROPS (Carboxymethylcellulose Sodium 0.5%) Recalled by Kilitch...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Health brand Lubricant Eye Drops (Propylene glycol 0.6%) Recalled by...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EQUATE brand Hydration PF Lubricant Eye Drops (Polyethylene glycol 400...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Health brand Recalled by Kilitch Healthcare India Limited Due to...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leader brand Lubricant Eye Drops (Carboxymethylcellulose Sodium 0.5%)...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leader brand Dry Eye Relief (Carboxymethylcellulose Sodium 1%) Recalled by...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rugby brand Polyvinyl Alcohol 1.4% Lubricating Eye Drops Recalled by Kilitch...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lubricant Gel Drops (Polyethylene glycol 400 0.4% Recalled by Kilitch...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lubricant Gel Drops (Carboxymethylcellulose sodium 1.0%) Recalled by Kilitch...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leader brand Dry Eye Relief (Polyethylene glycol 400 0.4% and Recalled by...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lubricant Eye Drops (Propylene glycol 0.6%) Recalled by Kilitch Healthcare...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KinderMed INFANTS' PAIN & FEVER Acetaminophen Recalled by KINDER FARMS LLC...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KinderMed KIDS' PAIN & FEVER Acetaminophen Recalled by KINDER FARMS LLC Due...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calibration Serum Level 3. CAL 3 Recalled by Randox Laboratories Ltd. Due to...
The Issue: There have been transcription errors on the Instructions For Use (IFU) of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORI REAL INTELLIGENCE Robotic Drill Recalled by Blue Belt Technologies, Inc...
The Issue: Possibility that the user is unable to resolve drill disconnection error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hookup Accessories used with MEDIVATORS ADVANTAGE PLUS and ADVANTAGE PLUS...
The Issue: Identification label on affected hookups could become illegible over time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.