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. 2,643 recalls have been distributed to Connecticut in the last 12 months.
Showing 4901–4920 of 28,245 recalls
Recalled Item: SmartPath to dStream for 1.5T. Model (REF) Numbers 781260 Recalled by...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Tornier Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V...
The Issue: The incorrect device is contained in the labeled package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Framegrabber card may not perform as intended. Monitor may show no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Framegrabber card may not perform as intended. Monitor may show no...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Disk Bay may not perform as intended. System may stop functioning and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Disk Bay may not perform as intended. System may stop functioning and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper Interventional Fluoroscopic X-ray Systems Recalled by...
The Issue: Dual In-Line Memory Modules (DIMMs) may not perform as intended. System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3:1 Dermacarrier Recalled by Zimmer Surgical Inc Due to Due to manufacturing...
The Issue: Due to manufacturing issue, the product is labeled as 3:1 ratio, but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MB215R - MILLS DUROGRIP TC Micro Needle Holder Recalled by Aesculap Inc Due...
The Issue: Needle Holder MB215R was inadvertently distributed as MB362R. Similarly,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MB362R - JACOBSON DUROGRIP TC Micro Needle Holder Recalled by Aesculap Inc...
The Issue: Needle Holder MB215R was inadvertently distributed as MB362R. Similarly,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Recalled by Philips North America Due to An incorrect electrical...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T Recalled by Philips North America Due to An incorrect...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T Recalled by Philips North America Due to An...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Recalled by Philips North America Due to An incorrect...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Conversion Recalled by Philips North America Due to An...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition X Recalled by Philips North America Due to An incorrect...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUABILITI AQUASTAT 0.9% Sodium Chloride Injection syringe Recalled by MRP,...
The Issue: The saline flush syringes may fail to meet USP criteria for stated sodium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Samsung Digital Diagnostic Mobile X-ray System Recalled by NeuroLogica...
The Issue: Mobile x-ray systems moving arm frame welding issue which presents the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.