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. 2,485 recalls have been distributed to Connecticut in the last 12 months.
Showing 19141–19160 of 28,245 recalls
Recalled Item: Professional Hospital Supply Recalled by Covidien LLC Due to Added...
The Issue: Added Instructions for Use: After application, inspect the Light Glove for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab Automation Modules Recalled by Siemens Healthcare Diagnostics, Inc....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ORCHESTRA Programmer A portable device Recalled by Sorin Group USA, Inc....
The Issue: Sorin Group USA, Inc. announces a voluntary field action for the ORCHESTRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation Modules Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Possible overheating of power cord plugs used to connect to FlexLab and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ORCHESTRA PLUS Programmer A portable device Recalled by Sorin Group USA,...
The Issue: Sorin Group USA, Inc. announces a voluntary field action for the ORCHESTRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thayer MiniSpacer Dual Spray MDI Adapter Counter Incrementing Actuator with...
The Issue: The insert and case label description of the device incorrectly reads...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum INFUSION PUMP with Master Drug Library Recalled by...
The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: sigma spectrum VOLUMETRIC INFUSION PUMP with Master Drug Library Recalled by...
The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V6 Rear Case Assembly Recalled by Baxter Healthcare Corp. Due to A...
The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS 4F Stiffened Micro-Introducer Recalled by Angiodynamics, Inc....
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Gender Solutions" Patellofemoral Joint Prosthesis Milling Handpiece...
The Issue: Complaints have been reported that the handpiece is inoperable. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4 Port "ON" Manifold (600 psi) w/4 ft. Transpac¿ IV Recalled by ICU Medical,...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOTECH Endoscope Cleaner and Reprocessor System 208V Recalled by Advanced...
The Issue: Advanced Sterilization Products (ASP) is recalling the EVOTECH Endoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRANSPAC¿ IV MONITORING KIT Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.