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. 2,221 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,221 in last 12 months

Showing 32213240 of 55,896 recalls

Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Hybrid MR IMRIS Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Hybrid (MC) Recalled by Baxter Healthcare Corporation...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter TruSystem 7500 Hybrid (SC) Recalled by Baxter Healthcare Corporation...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Hemopore 2PK nasal/sinus temporary wound dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore Standard 8cm fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore 4cm Standard 2PK fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore 8cm fragmentable nasal dressing Recalled by Stryker Corporation Due...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Stryker Corporation

Recalled Item: Nasopore Standard 4cm fragmentable nasal dressing Recalled by Stryker...

The Issue: There is a potential for blister seals on the product to present a bubble on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Stationary column TruSystem 7500 Recalled by Baxter Healthcare...

The Issue: There is a software issue which causes the upper back section to not be...

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

Class II — Potential Health HazardOngoing
DrugFebruary 25, 2025· MYLAN PHARMACEUTICALS INC

Recalled Item: Prasugrel Tablets Recalled by MYLAN PHARMACEUTICALS INC Due to Failed...

The Issue: Failed Dissolution Specifications - low dissolution results

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 25, 2025· A-S Medication Solutions LLC

Recalled Item: METFORMIN HYDROCHLORIDE EXTENDED- RELEASE 500MG Recalled by A-S Medication...

The Issue: Presence of Foreign Tablets/Capsules.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2025· Imprimis NJOF, LLC

Recalled Item: Tropicamide - Proparacaine - Phenylephrine - Ketorolac Sterile Ophthalmic...

The Issue: Sub-Potent Drug: The stability batch showed a subpotent result, which does...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 24, 2025· Denison Pharmaceuticals, LLC

Recalled Item: Zapzyt Recalled by Denison Pharmaceuticals, LLC Due to Chemical...

The Issue: Chemical Contamination: Presence of benzene.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 24, 2025· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....

The Issue: Device is missing the pin in the graft loader component.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2025· Checkpoint Surgical Inc

Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...

The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2025· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....

The Issue: Device is missing the pin in the graft loader component.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2025· Checkpoint Surgical Inc

Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...

The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline medical procedure kits, containing Medtronic Aortic Root Cannula

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medical convenience kits containing Medtronic Aortic Root Cannula are being...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medical convenience kits containing Medtronic Aortic Root Cannula are being...

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

Class I — Serious Health HazardOngoing