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 22361–22380 of 28,245 recalls
Recalled Item: Gyn Pack - contains Devon Light Glove Used during surgery Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minor Pack and Minor Pack II Pack - contains Devon Recalled by Stradis...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breast Pack - contains Devon Light Glove Used during surgery Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Basic Pack - contains Devon Light Glove Used during surgery Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laser Evlt Pack and Laser One Leg Evlt - contains Recalled by Stradis...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL Pack - contains Devon Light Glove Used during surgery Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Face Lift Pack - contains Devon Light Glove Used during surgery Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breast Augmentation Pack and Breast Augmentation Expanded Pack - contains...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Alignment Guide Recalled by Zimmer CAS Due to Zimmer CAS has...
The Issue: Zimmer CAS has determined that the potential exists for the spikes on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WEBSTER HIS Catheter Recalled by Biosense Webster, Inc. Due to The Webster...
The Issue: The Webster HIS catheter, 4Pole Fixed Curve with Auto ID, is not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal(R) Medium Specimen Retrieval Bag Recalled by DeRoyal Industries Inc...
The Issue: The firm received reports of specimen retrieval bags tearing, ripping, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultraview SL Command Modules Recalled by Spacelabs Healthcare Inc Due to...
The Issue: Ultraview SL Command Modules which were upgraded with the Masimo SpO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....
The Issue: The term DORSAL was laser etched on the incorrect side on some of the angled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....
The Issue: The term DORSAL was laser etched on the incorrect side on some of the angled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Recalled by Biomet, Inc. Due to Biomet hip...
The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....
The Issue: The term DORSAL was laser etched on the incorrect side on some of the angled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered HD Upgrade Set Recalled by BioHorizons Implant Systems Inc Due to...
The Issue: BioHorizons Tapered HD Upgrade set was packaged with an incorrect drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHALINX (TM) HAMMERTOE HANDLE Recalled by Wright Medical Technology, Inc....
The Issue: The term DORSAL was laser etched on the incorrect side on some of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MCK Maximum Congruent Knee System Recalled by Biomet, Inc. Due to Biomet hip...
The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mallory/Head Primary Hip System Recalled by Biomet, Inc. Due to Biomet hip...
The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.