Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,842 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,842 in last 12 months

Showing 86018620 of 55,896 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· 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
Medical DeviceSeptember 8, 2023· GE Healthcare

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

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
Medical DeviceSeptember 8, 2023· GE Medical Systems China Co., Ltd.

Recalled Item: F2-01 Frame Recalled by GE Medical Systems China Co., Ltd. Due to There is a...

The Issue: There is a potential interruption of data communication between E-modules...

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

Class II — Potential Health HazardOngoing
DrugSeptember 7, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Cequa (cyclosporine ophthalmic solution) 0.09% Recalled by SUN...

The Issue: Subpotent: Out of Specification result observed for low assay

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

Class III — Low RiskOngoing
Refund