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. 2,901 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,901 in last 12 months

Showing 12411260 of 55,896 recalls

Medical DeviceSeptember 30, 2025· CareFusion 303, Inc.

Recalled Item: Various models of BD Pyxis Pro 7-Drawer Auxiliary Recalled by CareFusion...

The Issue: Potential fluid ingress of anesthesia station or med station may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2025· IMPRIS Imaging Inc

Recalled Item: IMRIS Operating Suite Recalled by IMPRIS Imaging Inc Due to There is a...

The Issue: There is a potential safety issue associated with the magnet venting paths...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2025· IMPRIS Imaging Inc

Recalled Item: IMRIS Operating Suite Recalled by IMPRIS Imaging Inc Due to There is a...

The Issue: There is a potential safety issue associated with the magnet venting paths...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2025· CareFusion 303, Inc.

Recalled Item: All Serial Numbers/BD Pyxis CII Safe ES Tower Main Recalled by CareFusion...

The Issue: Potential fluid ingress of anesthesia station or med station may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2025· CareFusion 303, Inc.

Recalled Item: Various models of BD Pyxis Medbank: numbers: 1137-00 1145-00 Recalled by...

The Issue: Potential fluid ingress of anesthesia station or med station may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2025· B BRAUN MEDICAL INC

Recalled Item: Brand Name: Hemodialysis Bloodlines Product Name: STREAMLINE BLOODLINE SET...

The Issue: The potential for micro-air bubbles observed in the bloodline and...

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

Class I — Serious Health HazardOngoing
FoodSeptember 29, 2025· New Age International, Inc.

Recalled Item: Signature brand Enoki Mushroom Recalled by New Age International, Inc. Due...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 29, 2025· Medline Industries, LP

Recalled Item: Medline Recalled by Medline Industries, LP Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 29, 2025· Acella Pharmaceuticals, LLC

Recalled Item: Doxycycline Hyclate Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Failed dissolution specifications: Stability testing found that the lot did...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 29, 2025· Acuity Specialty Products, Inc.

Recalled Item: AFCO Recalled by Acuity Specialty Products, Inc. Due to cGMP deviations: The...

The Issue: cGMP deviations: The recall was initiated because required receipt testing...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 29, 2025· Acuity Specialty Products, Inc.

Recalled Item: Wyandotte Recalled by Acuity Specialty Products, Inc. Due to cGMP...

The Issue: cGMP deviations: The recall was initiated because required receipt testing...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 27, 2025· Vicky IT Inc.

Recalled Item: Bona Fish Recalled by Vicky IT Inc. Due to Fish is un-eviscerated (may be...

The Issue: Fish is un-eviscerated (may be contaminated with Clostridia botulinum), is...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 26, 2025· MAYEJ COMERCIALIZADORA S. de R.L. de C.V.

Recalled Item: Italian Parsley packaged in 24lb boxes Recalled by MAYEJ COMERCIALIZADORA S....

The Issue: pathogen Cyclospora cayetanensis

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 26, 2025· SLR Food Distribution, Inc.

Recalled Item: Wise Wife Ground Cinnamon Recalled by SLR Food Distribution, Inc. Due to...

The Issue: Contains elevated levels of lead

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2025· Dr. Reddy's Laboratories, Inc.

Recalled Item: Succinylcholine Chloride Injection Recalled by Dr. Reddy's Laboratories,...

The Issue: Out-of-Specification (OOS) result during the 6-month stability testing;...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 26, 2025· DSAART LLC

Recalled Item: Brand Name: AART Calf Implant Product Name: Calf Implant Model/Catalog...

The Issue: Due to manufactured products that deviated from established specifications...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· DSAART LLC

Recalled Item: Brand Name: AART Malar Implant Product Name: Malar Implant Model/Catalog...

The Issue: Due to manufactured products that deviated from established specifications...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· DSAART LLC

Recalled Item: Brand Name: AART Silicone Carving Implant Product Name: Silicone Carving...

The Issue: Due to manufactured products that deviated from established specifications...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· DSAART LLC

Recalled Item: Brand Name: AART Chin Implant Product Name: Chin Implant Model/Catalog...

The Issue: Due to manufactured products that deviated from established specifications...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· DSAART LLC

Recalled Item: Brand Name: AART Pectoral Implant Product Name: Pectoral Implant...

The Issue: Due to manufactured products that deviated from established specifications...

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

Class II — Potential Health HazardOngoing