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. 993 recalls have been distributed to Connecticut in the last 12 months.
Showing 31961–31980 of 51,038 recalls
Recalled Item: Southeastern Mills Recalled by Southeastern Mills Custom Seasoning Solutions...
The Issue: Products were manufactured from raw material (buttermilk solids) that may...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: buPROPion Hydrochloride Extended-release Tablets Recalled by Sun...
The Issue: Failed Dissolution Specifications; 18 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...
The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...
The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...
The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...
The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril tablets Recalled by Accord Healthcare, Inc. Due to Failed...
The Issue: Failed tablet/capsule specification: missing break line on the 5mg tablet.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-release Tablets Recalled by Sun...
The Issue: Failed Dissolution Specifications; 18 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eclipse Hypodermic Needle Recalled by Becton Dickinson & Company Due to BD...
The Issue: BD is initiating a Product Advisory for the Eclipse Hypodermic Needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Reverse Shoulder System Humeral Tray Model 115340 Recalled by...
The Issue: Higher than anticipated rate of fracturing due to design. Risk of revision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aripiprazole Tablets Recalled by Apotex Inc. Due to Superpotent Drug:...
The Issue: Superpotent Drug: Product may not meet specifications throughout shelf life.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gonsalves Sugar Coated Almonds Recalled by The Henry Gonsalves Co. Due to...
The Issue: Product contains undeclared wheat, Red #3, Red #40, Blue #1, Yellow # 6
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Active Articulation ArComXL Polyethylene Bearings Active Articulation...
The Issue: Product complaints indicated that the part and lot numbers on the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Beckman Coulter has determined that additional clarification for the Blast...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 9800. MDL Numbers: D222250 Recalled by GE OEC Medical Systems, Inc Due...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The OEC 9900 Elite mobile fluoroscopy system is designed to Recalled by GE...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall...
The Issue: Product complaints indicated that the part and lot numbers on the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniLoc¿ Safety Infusion Set Winged without Y-Injection Site. Product Code:...
The Issue: Bard Access Systems announces a voluntary field action for the SafeStep¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter Inc....
The Issue: Beckman Coulter has determined that additional clarification for the Blast...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeStep¿ Huber Needle Set with Y-Injection Site. Product Code: LH-0029YN....
The Issue: Bard Access Systems announces a voluntary field action for the SafeStep¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.