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. 2,659 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,659 in last 12 months

Showing 2376123780 of 55,896 recalls

Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Enteric Bacterial Panel EU Recalled by Becton Dickinson & Co. Due...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max MRSA XT Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Enteric Parasite Panel EU Recalled by Becton Dickinson & Co. Due...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max GC RT PCR Assay Recalled by Becton Dickinson & Co. Due to The...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK TNA 2 Recalled by Becton Dickinson & Co. Due to The foil bags...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max ExK DNA 1 EU LUO Recalled by Becton Dickinson & Co. Due to The...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2019· Becton Dickinson & Co.

Recalled Item: Kit BD Max Enteric Viral Panel EU Catalog # 443985 Recalled by Becton...

The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...

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

Class II — Potential Health HazardOngoing
DrugJuly 17, 2019· Macleods Pharma Usa Inc

Recalled Item: Tamsulosin Hydrochloride Capsules Recalled by Macleods Pharma Usa Inc Due to...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Nystatin and Triamcinolone Acetonide Cream USP100 Recalled by Lupin...

The Issue: Failed Content Uniformity Specifications: Out-of-specification result...

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

Class III — Low RiskOngoing
Refund
DrugJuly 17, 2019· ImprimisRx NJ

Recalled Item: Timolol- Dorzolamide- Latanoprost P-F (0.5/2.0/0.005%) ophthalmic drops...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 17, 2019· ImprimisRx NJ

Recalled Item: Timolol-Latanoprost P-F (0.5/0.005%) ophthalmic drops Recalled by ImprimisRx...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2019· Deva Holding AS - Cerkezkoy Subesi

Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...

The Issue: CGMP Deviations: product was manufactured that did not prevent possible...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2019· Deva Holding AS - Cerkezkoy Subesi

Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...

The Issue: CGMP Deviations: product was manufactured that did not prevent possible...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2019· Deva Holding AS - Cerkezkoy Subesi

Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...

The Issue: CGMP Deviations: product was manufactured that did not prevent possible...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2019· Deva Holding AS - Cerkezkoy Subesi

Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...

The Issue: CGMP Deviations: product was manufactured that did not prevent possible...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2019· Deva Holding AS - Cerkezkoy Subesi

Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...

The Issue: CGMP Deviations: product was manufactured that did not prevent possible...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2019· Deva Holding AS - Cerkezkoy Subesi

Recalled Item: Temozolomide Capsules Recalled by Deva Holding AS - Cerkezkoy Subesi Due to...

The Issue: CGMP Deviations: product was manufactured that did not prevent possible...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 16, 2019· Bionpharma Inc.

Recalled Item: Clobazam Oral Suspension Recalled by Bionpharma Inc. Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: Out-of-specification...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 16, 2019· Philips North America, LLC

Recalled Item: Philips Azurion systems with software version R1.2 -Interventional...

The Issue: The cold restart of Azurion R1.2 systems may take up to 7 minutes if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2019· TeDan Surgical Innovations LLC

Recalled Item: Fukushima suction tubes Recalled by TeDan Surgical Innovations LLC Due to...

The Issue: There was incorrect raw material used in the production of the identified lot.

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

Class II — Potential Health HazardOngoing