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. 2,619 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,619 in last 12 months

Showing 3408134100 of 55,896 recalls

Medical DeviceMarch 17, 2017· Smiths Medical ASD Inc.

Recalled Item: CADD¿ Administration Set Recalled by Smiths Medical ASD Inc. Due to Smiths...

The Issue: Smiths Medical has become aware that the drawing on the Instructions for Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2017· Medtronic Neuromodulation

Recalled Item: DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation Recalled...

The Issue: Medtronic received reports that the DBS depth stop did not adequately secure...

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

Class II — Potential Health HazardOngoing
DrugMarch 17, 2017· Shire

Recalled Item: Kalbitor (ecallantide) Recalled by Shire Due to Presence of Particulate...

The Issue: Presence of Particulate Matter: Glass

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2017· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Fluocinonide Cream UPS Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...

The Issue: Cross contamination with other products: Certain lots of Fluocinonide Cream...

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

Class III — Low RiskOngoing
Refund
DrugMarch 17, 2017· Akorn, Inc.

Recalled Item: LATANOPROST OPHTHALMIC SOLUTION Recalled by Akorn, Inc. Due to Lack of...

The Issue: Lack of assurance of sterility: product was found to be empty, under-filled,...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 16, 2017· Allergan Sales, LLC

Recalled Item: Lumigan (bimatoprost ophthalmic solution) 0.01% Recalled by Allergan Sales,...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugMarch 16, 2017· Fresenius Kabi USA, LLC

Recalled Item: Fluphenazine Decanoate Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Cataract Kit Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Eye Cataract Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Custom Tray Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Vitrectomy Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Zimmer Biomet Spine, Inc

Recalled Item: Altius M-INI OCT Posterior Spinal Fixation System Recalled by Zimmer Biomet...

The Issue: Zimmer Biomet is recalling the Altius M-INI OCT Posterior Spinal Fixation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Vitrectomy Kit Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Cataract Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Setup Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Lasik Tray Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: ENT Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Cataract Kit - Dr. Slingsby Recalled by Windstone Medical Packaging, Inc....

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Dicken Eye Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Ophthalmic Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing