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. 2,873 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,873 in last 12 months

Showing 42414260 of 55,896 recalls

DrugNovember 4, 2024· Boulla LLC

Recalled Item: PeakMax Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 4, 2024· Boulla LLC

Recalled Item: ZoomMax Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: Mammotrak Interventional Coil 3.0T Recalled by Philips North America Llc Due...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CI Analyzer. Catalog Numbers: 10947347. Recalled by Siemens...

The Issue: Potential that the IMT Diluent volume remaining (% remaining) does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Straight Smile, LLC

Recalled Item: BYTE Aligner System BYTE All-Day Aligner System BYTE Recalled by Straight...

The Issue: Virtual-only clinical workflow utilized for dental aligners and impression...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: SENSE Breast Coil 3.0T 7ch Recalled by Philips North America Llc Due to...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: dS Breast 16ch 1.5T Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: Mammotrak Diagnostic Coil 1.5T Recalled by Philips North America Llc Due to...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: dS Breast 7ch 3.0T Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: ST SENSE Breast Dx Coil Recalled by Philips North America Llc Due to...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: SENSE Breast Coil Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: dS Breast 7ch 1.5T Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: dS Breast 16ch 3.0T Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: ST SENSE Breast Coil Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: Mammotrak Interventional Coil 1.5T Recalled by Philips North America Llc Due...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: Mammotrak Diagnostic Coil 3.0T Recalled by Philips North America Llc Due to...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: Achieva TX Interventional Coil 3.0T Recalled by Philips North America Llc...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
FoodNovember 1, 2024· GRIFFITH FOODS LTD

Recalled Item: Item 42081001 Recalled by GRIFFITH FOODS LTD Due to potential for pieces of...

The Issue: potential for pieces of metal in product

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2024· GRIFFITH FOODS LTD

Recalled Item: Item 16354301 Recalled by GRIFFITH FOODS LTD Due to potential for pieces of...

The Issue: potential for pieces of metal in product

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2024· GRIFFITH FOODS LTD

Recalled Item: Item 25293502 Recalled by GRIFFITH FOODS LTD Due to potential for pieces of...

The Issue: potential for pieces of metal in product

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

Class II — Potential Health HazardOngoing
Refund