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 861880 of 30,153 recalls

Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Plastic Blood Gas Capillary Tubes Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Plastic Blood Gas Capillary Tubes Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL MicroHematocrit Capillary Tubes Recalled by ASP Global, LLC. dba...

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL End Caps for SAFE-T-FILL Blood Gas Capillaries Recalled by ASP...

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· Synthes (USA) Products LLC

Recalled Item: LOW PROF LCKNG SCREW Recalled by Synthes (USA) Products LLC Due to Although...

The Issue: Although the etched length on the screw is correct, the length marked on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· GE Healthcare Finland Oy

Recalled Item: Carescape B450 Recalled by GE Healthcare Finland Oy Due to Potential loss of...

The Issue: Potential loss of monitoring on affected monitors when powered by certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: CODMAN Disposable Perforator 9mm. Cranial Perforator. Recalled by Integra...

The Issue: Expansion of recall of size 14 mm Codman Disposable Perforators for...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 26, 2025· DSAART LLC

Recalled Item: Brand Name: AART Gluteal Implant Product Name: Gluteal 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
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 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 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 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 25, 2025· Covidien, LP

Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm...

The Issue: A manufacturing issue could lead to a malformed cover tube press which can...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2025· BALT USA, LLC

Recalled Item: Brand Name: MEGA Ballast Distal Access Platform Product Name: Mega Recalled...

The Issue: Due to an identified manufacturing defect involving coating material lifting...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 25, 2025· Covidien, LP

Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm...

The Issue: A manufacturing issue could lead to a malformed cover tube press which can...

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

Class II — Potential Health HazardOngoing