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. 2,445 recalls have been distributed to Connecticut in the last 12 months.
Showing 25741–25760 of 28,245 recalls
Recalled Item: GE Healthcare Discovery IGS 730 Cardiovascular X-Ray Imaging System. The...
The Issue: GE Healthcare has recently become aware of a potential safety issue with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX FEMORAL FIXATION SYSTEM COMPRESSION LAG SCREW Recalled by Zimmer,...
The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 and Dimension Vista 1500 System Aliquot Well Recalled by...
The Issue: Siemens is conducting a field correction for Dimension Vista 500 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeShield Recalled by Hospira Inc. Due to Hospira has received reports of...
The Issue: Hospira has received reports of customers experiencing air-in-line alarms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CHAMPION Medical Recliner Recalled by Invacare Corporation Due to There is a...
The Issue: There is a possibility of elevated temperatures in the seat pad. In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene BC-GN Kit (Catalog number 20-005-021) Recalled by Nanosphere, Inc....
The Issue: There is a specific Extraction Tray lot containing Tips that may slightly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit Recalled by CareFusion 303, Inc. Due to CareFusion is...
The Issue: CareFusion is recalling the Alaris PC units model 8015 (PC unit), version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene BC-GP Kit (Catalog number 20-005-018) Recalled by Nanosphere, Inc....
The Issue: There is a specific Extraction Tray lot containing Tips that may slightly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The SurgiCounter Charging Cradle Product Usage: SurgiCounter Charging...
The Issue: Faulty SurgiCounter Charging Cradle can prevent the scanner from charging or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.