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. 2,889 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,889 in last 12 months

Showing 17611780 of 55,896 recalls

FoodAugust 8, 2025· SUNGAL INC

Recalled Item: UDK Recalled by SUNGAL INC Due to Cyclamate adulteration

The Issue: Cyclamate adulteration

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
DrugAugust 8, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Theophylline extended-release tablets 400mg Recalled by Glenmark...

The Issue: Failed Dissolution Specifications: Failure results (above) were reported for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 8, 2025· Greiner Bio-One North America, Inc.

Recalled Item: Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2% Recalled...

The Issue: Blood collection tubes were manufactured with the label applied too high on...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· Schiller, Ag

Recalled Item: Argus PB-3000 Recalled by Schiller, Ag Due to Vital sign monitoring...

The Issue: Vital sign monitoring instrument may trigger an error message during blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· Baxter Healthcare Corporation

Recalled Item: Baster Continu-Flo Solution Set Recalled by Baxter Healthcare Corporation...

The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· Philips Medical Systems Nederland B.V.

Recalled Item: IntelliSpace Cardiovascular Recalled by Philips Medical Systems Nederland...

The Issue: Software issue that results in the display of outdated information.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 11B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 8B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 11A...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 9B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 6 Service...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 10B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 12A...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 7 Recalled...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 2023B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
FoodAugust 7, 2025· Wang Globalnet

Recalled Item: (Bulk) Oyster Recalled by Wang Globalnet Due to Oyster product potentially...

The Issue: Oyster product potentially contaminated with Norovirus

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 7, 2025· Flosonics Medical (R/A 1929803 ONTARIO CORP.)

Recalled Item: FloPatch FP120 Recalled by Flosonics Medical (R/A 1929803 ONTARIO CORP.) Due...

The Issue: Flowmeter patch as a human readable expiry date on the outer shipping...

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

Class III — Low RiskOngoing