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. 1,816 recalls have been distributed to Connecticut in the last 12 months.
Showing 40421–40440 of 51,038 recalls
Recalled Item: CooperSurgical Infant Heel Gel Warmers Recalled by CooperSurgical, Inc. Due...
The Issue: Products without expiration date have the remote potential for minor burn
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compounded Plaquex Recalled by AnazaoHealth Corporation Due to Good...
The Issue: Good Manufacturing Practices Deviations: The product has an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AMPD GOLD Bee Pollen capsules Recalled by Detox Transforms Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: iNDiGO capsules Recalled by Detox Transforms Due to Undeclared Phenolphthalein
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BtRiM Max capsules Recalled by Detox Transforms Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EDGE Amplified Weight Release capsules Recalled by Detox Transforms Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: iNSANE Bee Pollen capsules Recalled by Detox Transforms Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHILI POWDER 50 LBS Recalled by Wm. E. Martin & Sons Co., Inc. Due to...
The Issue: Cumin contains undeclared peanut protein
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GROUND CUMIN STERILE TREATED PROD. OF TURKEY Recalled by Wm. E. Martin &...
The Issue: Cumin contains undeclared peanut protein
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PROBAR Frosted Peanut Butter BASE Protein Bar Recalled by Probar LLC Due to...
The Issue: PROBAR, LLC has initiated a voluntary recall of its PROBAR Base Frosted...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicardipine Hydrochloride Injection Recalled by Mylan Institutional LLC Due...
The Issue: Subpotent Drug and Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Passport V Monitor Recalled by Mindray DS USA, Inc. dba Mindray North...
The Issue: An issue has been identified with Passport V Monitors invasive blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAX-TL 9.0 x 7.0 mm Implant Recalled by Southern Implants, Inc Due to Z-MAX...
The Issue: Z-MAX Implant, 9mm diameter, 7mm length labeled package, catalog number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Caps for capillary 140/175 uL Recalled by Siemens...
The Issue: Capillary Caps for RAPIDLyte Multicap and Multicap-S Blood Collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Restoris Partial Knee Application (PKA) RIO (TGS 2.0). For use Recalled by...
The Issue: When using the MAKOplasty partial knee Arthroplasty application, the burr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FORUM Archive and Viewer Recalled by Carl Zeiss Meditec AG Due to Software...
The Issue: Software defect in the FORUM Viewer versions 3.1 and 3.2 which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Caps for capillary 100 uL Recalled by Siemens Healthcare...
The Issue: Capillary Caps for RAPIDLyte Multicap and Multicap-S Blood Collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Caps for capillary 50/60 uL Recalled by Siemens...
The Issue: Capillary Caps for RAPIDLyte Multicap and Multicap-S Blood Collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.