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. 2,643 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,643 in last 12 months

Showing 46414660 of 51,038 recalls

Medical DeviceAugust 20, 2024· Ossur H / F

Recalled Item: Miami J Select Collar Recalled by Ossur H / F Due to Pressure sensitive...

The Issue: Pressure sensitive adhesive hooks attached to the sides of the anterior...

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

Class II — Potential Health HazardOngoing
DrugAugust 20, 2024· Elevate Oral Care

Recalled Item: Just Right 5000 Recalled by Elevate Oral Care Due to LABELING: LABEL MIX-UP.

The Issue: LABELING: LABEL MIX-UP.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: DiamondTOUCH Digital Inflation Device Recalled by Merit Medical Systems,...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: basixTOUCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: Custom Inflation Kit Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: basixSKY Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: MONARCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: BlueFIRE Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: Blue Diamond Digital Inflation Device Recalled by Merit Medical Systems,...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: basixTOUCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: StabiliT TOUCH Syringe Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: IntelliSystem Inflation Device Recalled by Merit Medical Systems, Inc. Due...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Hologic Inc

Recalled Item: Selenia Dimensions/ 3Dimensions-Digital breast tomosynthesis Software...

The Issue: Identified an issue with Selenia Dimensions 1.12.0 and 3Dimensions 2.3.0...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Tonsil ENT Pack that contains the Recalled by Windstone...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Septo Pack that contains the Cardinal Recalled by Windstone...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Tonsil Pack that contains the Cardinal Recalled by Windstone...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical T and A Pack that contains Recalled by Windstone Medical...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Tonsil Tray that contains the Cardinal Recalled by Windstone...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2024· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module Model 8100 Recalled by CareFusion 303, Inc. Due to Due to...

The Issue: Due to affected devices that may have bent female IUI connector and may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2024· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Redwood 1.0 and 2.0 Diagnostic Ultrasound Systems Recalled by Siemens...

The Issue: If ultrasound systems with software, are changed from factory default to :...

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

Class II — Potential Health HazardOngoing