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. 2,748 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,748 in last 12 months

Showing 1592115940 of 55,896 recalls

FoodNovember 8, 2021· GIVE AND GO

Recalled Item: Favorite Day Bakery Frosted Sugar Cookies 13.5 oz. Recalled by GIVE AND GO...

The Issue: Potential for metal in product

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 8, 2021· GIVE AND GO

Recalled Item: two-bite apple caramel cupcakes 10 oz. Recalled by GIVE AND GO Due to...

The Issue: Potential for metal in product

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 8, 2021· Boston Scientific Corporation

Recalled Item: Boston Scientific ROTAPRO Recalled by Boston Scientific Corporation Due to...

The Issue: Manufacturing instructions did not include the directions to not retest the...

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

Class II — Potential Health HazardOngoing
FoodNovember 5, 2021· ILG International Trading, Inc.

Recalled Item: Natural Delight Collection Natural Dried Apricots Recalled by ILG...

The Issue: Product contains undeclared sulfites.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 5, 2021· Dignitana, Inc.

Recalled Item: DigniCap Delta Scalp Cooling System Recalled by Dignitana, Inc. Due to...

The Issue: Instructions for Use (IFUs) updated to include use of a headband is now...

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

Class II — Potential Health HazardOngoing
DrugNovember 4, 2021· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Flocinolone Acetonide 0.01% Topical Oil Recalled by Amneal Pharmaceuticals...

The Issue: Subpotent Drug: Out-of-specification assay result was obtained for...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2021· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Flocinolone Acetonide 0.01% Topical Oil Recalled by Amneal Pharmaceuticals...

The Issue: Subpotent Drug: Out-of-specification assay result was obtained for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· Migo Trading LLC

Recalled Item: FLOWFLEX SARS-COV-2 Antigen Rapid Test (Self-Testing) Recalled by Migo...

The Issue: Devices are determined to be inconsistent with the firm's Emergency Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· Medtronic Neuromodulation

Recalled Item: Medtronic Wireless Recharger Model WR9200 included in the RS7200 Recharger...

The Issue: The wireless rechargers (WR; WR9200 and WR9220; included in the Recharger...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing