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. 2,664 recalls have been distributed to Connecticut in the last 12 months.
Showing 3061–3080 of 28,245 recalls
Recalled Item: Ingenia 3.0T - For use as a diagnostic device to obtain cross-sectional...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition S - For use as a diagnostic device Recalled by Philips...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T CX - For use as a diagnostic device Recalled by Philips North...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution Upgrade 3.0T - For use as a diagnostic device Recalled by Philips...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X- For use as a diagnostic device to Recalled by Philips...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T - For use as a Recalled by Philips North...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition X - For use as a diagnostic device Recalled by Philips...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T -For use as a diagnostic device to obtain cross-sectional...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to Ingenia Elition X - For use as a Recalled by Philips North...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S -For use as a diagnostic device to Recalled by Philips...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 5300 - For use as a diagnostic device to obtain cross-sectional images...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 7700 -For use as a diagnostic device to obtain cross-sectional images...
The Issue: Integrated Radio Frequency (IRF) Carrier assembly screws may come loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 (LP15) Model/Catalog Numbers: o 97577-000101 o 99577-000046 o...
The Issue: Due to an out of tolerance tool being used on monitor/defibrillator systems.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Predict+ is a data-driven Recalled by Blue Ortho Due to Predict+ is being...
The Issue: Predict+ is being recalled for lack of pre-market clearance/approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Melrose Wakefield Hospital Injector And Syringe Recalled by Merit Medical...
The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Inflation Device 30 atm/bar MAP152 AssessPLUS Large Bore Hemostasis...
The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Inflation Device 30 atm/bar Injector And Syringe Recalled by Merit...
The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Inflation Device 30 atm/bar MAP403 MBA Hemostasis Valve Metal...
The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Inflation Device 30 atm/bar MAP302 Honor Hemostasis Valve Metal...
The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE Automatic Digital Blood Pressure Monitor Recalled by MEDLINE...
The Issue: It has been determined that certain Blood Pressure Monitors containing a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.