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. 2,623 recalls have been distributed to Connecticut in the last 12 months.

51,038 total recalls
2,623 in last 12 months

Showing 79818000 of 51,038 recalls

Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· Stryker Corporation

Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...

The Issue: An error was identified on the expiration date of the product label. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2023· EITAN MEDICAL LTD

Recalled Item: Sapphire Infusion Pumps Recalled by EITAN MEDICAL LTD Due to Infusion Pumps...

The Issue: Infusion Pumps with affected software revision may fail to detect air in...

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

Class I — Serious Health HazardOngoing
DrugSeptember 8, 2023· Church & Dwight Inc

Recalled Item: TheraBreath for Kids! Oral Rinse Recalled by Church & Dwight Inc Due to...

The Issue: Microbial contamination of Non-Sterile Product; presence of yeast identified...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 8, 2023· Novartis Pharmaceuticals Corp.

Recalled Item: SANDIMMUNE Oral Solution (cyclosporine oral solution Recalled by Novartis...

The Issue: Crystallization: bottles of Sandimmune Oral Solution were determined to...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 8, 2023· GE Healthcare

Recalled Item: Universal Viewer Workflow Manager Recalled by GE Healthcare Due to When...

The Issue: When using Universal Viewer or Centricity Universal Viewer with Workflow...

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

Class II — Potential Health HazardOngoing