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. 936 recalls have been distributed to Connecticut in the last 12 months.
Showing 48541–48560 of 51,038 recalls
Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Surgical Bed Recalled by Stryker Medical Division of Stryker...
The Issue: Stryker Medical Model 3002S3EX and Model 3005S3EX beds built between March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical microscope The device is used to improve the visibility Recalled by...
The Issue: The brake in the Z axis and/or brakes in the AB and C axes failed during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical microscope The device is used to improve the visibility Recalled by...
The Issue: The brake in the Z axis and/or brakes in the AB and C axes failed during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech Medical Instrument Corporation Macro Micro Subdural Electrode. For...
The Issue: The microelectrodes are not flush with the silastic substrate, may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Surgical Bed Recalled by Stryker Medical Division of Stryker...
The Issue: Stryker Medical Model 3002S3EX and Model 3005S3EX beds built between March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...
The Issue: Small holes (approximately 1 mm or less) found in device unit level...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zicam Extreme Congestion Relief (oxymetazoline HCl) nasal gel Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products: Product may be contaminated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Taztia XT(diltiazem HCI extended release capsules Recalled by Watson...
The Issue: Failed Dissolution Specification: Out of a specification result occurred...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Flanax (aluminum hydroxide Recalled by Belmora LLC Due to Defective...
The Issue: Defective Container: Product lacks tamper evident breakaway band on cap.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mojo nights SUPREME Capsules Recalled by Performance Plus Marketing, Inc....
The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLUE Diamond Pill Recalled by Performance Plus Marketing, Inc. Due to...
The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLUE Diamond PLATINUM Capsules Recalled by Performance Plus Marketing, Inc....
The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mojo nights Capsules Recalled by Performance Plus Marketing, Inc. Due to...
The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CASANOVA Capsules Recalled by Performance Plus Marketing, Inc. Due to...
The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.