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.

51,038 total recalls
2,445 in last 12 months

Showing 2636126380 of 51,038 recalls

Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature sensor Foley catheter 18FR Recalled by Degania Silicone, Ltd....

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature Sensor Catheter 14FR Recalled by Degania Silicone, Ltd. Due to...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Foley Catheter with temperature sensor 400TM 18FR Recalled by Degania...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Thermistor Foley catheter Recalled by Degania Silicone, Ltd. Due to The...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature sensor Foley catheter 8FR Recalled by Degania Silicone, Ltd. Due...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Thermistor Foley catheter Recalled by Degania Silicone, Ltd. Due to The...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature sensing catheter 16FR Recalled by Degania Silicone, Ltd. Due to...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature Sensor Catheter 8FR Recalled by Degania Silicone, Ltd. Due to...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with...

The Issue: Medtronic has become aware of a potential for loss of high voltage and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Percepta CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm and...

The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic EnTrust Escudo D144VRC (OUS distribution) Product Usage: The...

The Issue: Medtronic has become aware of a potential for loss of high voltage and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with...

The Issue: Medtronic has become aware of a potential for loss of high voltage and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with...

The Issue: Medtronic has become aware of a potential for loss of high voltage and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic EnTrust Escudo D144DRG (OUS distribution) Product Usage: The...

The Issue: Medtronic has become aware of a potential for loss of high voltage and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with...

The Issue: Medtronic has become aware of a potential for loss of high voltage and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Percepta Quad CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm...

The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Percepta Quad CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm...

The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Percepta CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm and...

The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...

The Issue: The flow rate test verification was not properly executed for certain Sigma...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing