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. 2,529 recalls have been distributed to Connecticut in the last 12 months.
Showing 16001–16020 of 28,245 recalls
Recalled Item: EasyTouch (ET) Insulin Syringe 29G 0.5ml ¿" (Item 829555) Product Recalled...
The Issue: The retail shelf cartons may be labeled with an incorrect lot number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyTouch (ET) Insulin Syringe 29G 1ml ¿" (Item 829155) Product Recalled by...
The Issue: The retail shelf cartons may be labeled with an incorrect lot number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec HeartMate 3 LVAS Implant Kit Recalled by Abbott Due to Reports of...
The Issue: Reports of outflow graft twist occlusions. Patients whose devices experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELLSEARCH¿ CIRCULATING Tumor Cell Kits (IVD) (Product Code 7900001)...
The Issue: Unusually high number of total images/unassigned events may require...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein CU 1000 Halogen Curing Light Recalled by Handpiece Headquarters...
The Issue: Tip of the curing light was too hot causing a heat sensation in the patients.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS IMRI 1.5T AND 3T S System Product Usage: The Recalled by Deerfield...
The Issue: The DC power to the IFOSS collision detector control panel at your facility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas e 801 immunoassay analyzer Recalled by Roche Diagnostics Corporation...
The Issue: The syringe plunger on the device may be mounted in a tilted position, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Salvage System (OSS) Modular Arthrodesis 0 Degree Locking Collar...
The Issue: There is a potential dry blast irregularity on the locking collar screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Retractor f/Sciatic Nerve Long Recalled by Synthes (USA) Products LLC Due to...
The Issue: There is a potential for microspores to form on the hollow handle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Head Component Recalled by Zimmer Biomet, Inc. Due to Two lots of...
The Issue: Two lots of different sized modular heads potentially commingled. Risks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Retractor f/Sciatic Nerve Recalled by Synthes (USA) Products LLC Due to...
The Issue: There is a potential for microspores to form on the hollow handle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PR4100 Microplate Reader US Recalled by Bio-Rad Laboratories Inc Due to The...
The Issue: The connector of the power supply was capable of fitting other components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Head Component Recalled by Zimmer Biomet, Inc. Due to Two lots of...
The Issue: Two lots of different sized modular heads potentially commingled. Risks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T2100 Micro flex Drive Treadmill Recalled by GE Medical Systems Ultrasound &...
The Issue: A performance issue with customer owned spare parts, T2100 Microflex drive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 CryoBalloon Focal Catheter Recalled by PENTAX of America Inc Due to The...
The Issue: The catheter alignment arrow printed onto the strain relief is not aligned...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.