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. 2,664 recalls have been distributed to Connecticut in the last 12 months.
Showing 2661–2680 of 28,245 recalls
Recalled Item: Convertor Isolation Gown Recalled by Cardinal Health 200, LLC Due to...
The Issue: Isolation Gowns were manufactured with raw materials that may fail the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Server Software Versions 11.1.4 through 11.1.6 Recalled by Securitas...
The Issue: Certain software versions will not notify end users of calls initiated by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD COR GX Instrument Version or Model: 443990 Catalog Number: 443990...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Synapsys Informatics Solution (Laboratory Solution) Version or Model:...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC FX Recalled by Becton Dickinson & Co. Due to BD confirmed that...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hybrid Recon software on Hermes Medical Imaging Suite version 6.1 Recalled...
The Issue: Due a potential software/configuration issue that may result is incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MAX System Recalled by Becton Dickinson & Co. Due to BD confirmed that...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cartiva Synthetic Cartilage Implant (SCI) Catalog: CAR-06-US (6mm) Recalled...
The Issue: Patients implanted with synthetic cartilage implant, may experience a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD EpiCenter Single User Software Version or Model: 441007 Catalog Recalled...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD EpiCenter Data Management System Recalled by Becton Dickinson & Co. Due...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number:...
The Issue: High-level disinfection ("HLD") with Acecide-C disinfectant in the Olympus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BACTEC 9240 System Version or Model: 445475 Catalog Number: 445475 Recalled...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD COR MX Instrument Version or Model: 443989 Catalog Number: 443989...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD EpiCenter Data Management System Version or Model: 440887 Catalog...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD COR PX Instrument Version or Model: 443988 Catalog Number: 443988...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC FX40 Instrument Version or Model: 442296 Catalog Number: 442296...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BACTEC 9120 System Version or Model: 445570 Catalog Number: 445570 Recalled...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix M50 Automated Microbiology System Version or Model: 443624...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Offset Cup Impactor - 3/8-16 interface. Reusable surgical instrument used...
The Issue: Recalled lot does not meet specification and has reported incidents of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Daytona Small Stature Product Name: CoCr LockingCap 4.5mm...
The Issue: Due to manufacturing defects observed on Locking Caps that affect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.