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. 966 recalls have been distributed to Connecticut in the last 12 months.
Showing 40921–40940 of 51,038 recalls
Recalled Item: RotoRest Delta Advanced Therapy System. The RotoRest Delta Advanced Kinetic...
The Issue: The recalled devices labeling and instructions for use contain unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Pediatric Direct-Wired Disposable Defibrillation/Pacing...
The Issue: The firm discovered that during the use of these defibrillation electrodes a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cable remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...
The Issue: Complaints have been reported of unintended movement occurring during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IR remote control JUPITER / TS7500 Recalled by Trumpf Medical Systems, Inc....
The Issue: Complaints have been reported of unintended movement occurring during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cable remote control JUC Recalled by Trumpf Medical Systems, Inc. Due to...
The Issue: Complaints have been reported of unintended movement occurring during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IR remote control JUX Recalled by Trumpf Medical Systems, Inc. Due to...
The Issue: Complaints have been reported of unintended movement occurring during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriaDyne Proventa Critical Care Therapy System. The TriaDyne Proventa...
The Issue: The recalled devices labeling and instructions for use contain unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IR remote control JUPITER U Recalled by Trumpf Medical Systems, Inc. Due to...
The Issue: Complaints have been reported of unintended movement occurring during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IR remote control JUC Recalled by Trumpf Medical Systems, Inc. Due to...
The Issue: Complaints have been reported of unintended movement occurring during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (R)Cable remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due...
The Issue: Complaints have been reported of unintended movement occurring during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q Recalled by Siemens Medical Solutions USA, Inc Due to Suboptimal...
The Issue: Suboptimal routing of the cable may result in increased wear over time....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IIR remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...
The Issue: Complaints have been reported of unintended movement occurring during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cable remote control JUPITER / TS7500 Recalled by Trumpf Medical Systems,...
The Issue: Complaints have been reported of unintended movement occurring during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cable remote control JUPITER U Recalled by Trumpf Medical Systems, Inc. Due...
The Issue: Complaints have been reported of unintended movement occurring during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MitoXANTRONE Injection Recalled by Hospira Inc. Due to Failed Stability...
The Issue: Failed Stability Specifications: Product is subpotent and has out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility; improperly crimped fliptop vials
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens Linear Accelerator: ARTISTE Recalled by Siemens Medical Solutions...
The Issue: Use of any unauthorized third-party components on Siemens LINACs may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PureLife Naturals Adult Multi-Plus Multi-Vitamins & Minerals Plus Herbs...
The Issue: Labels indicate "no wheat" "no gluten" and the products contain gluten and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PureLife Naturals Multi-Action Immunity 90 Pure-Caps HDPE bottle Recalled by...
The Issue: Labels indicate "no wheat" "no gluten" and the products contain gluten and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole Foods Tarte Aux Pomme 10 inch Recalled by Whole Food Market Due to...
The Issue: Product contains undeclared almonds
Recommended Action: Do not consume. Return to store for a refund or discard.