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 2704127060 of 55,896 recalls

Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors Recalled by The...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: ExactaMix Recalled by The Metrix Company Due to Potential for leaking product

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· The Metrix Company

Recalled Item: SECURE EVA - DUAL CHAMBER CONTAINER with Manifold Recalled by The Metrix...

The Issue: Potential for leaking product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· Zimmer Biomet, Inc.

Recalled Item: StageOne Hip Recalled by Zimmer Biomet, Inc. Due to There is a potential for...

The Issue: There is a potential for comingling of the 43MM and 51 MM molds

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· DePuy Orthopaedics, Inc.

Recalled Item: CORAIL AMT COXA VARA NECK SEGMENT (KLA) Pro. Code L20432 Recalled by DePuy...

The Issue: There is the potential for debris/material to be found behind the O-rings in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2018· Encore Medical, Lp

Recalled Item: Exprt Precision System: Revision Hip Recalled by Encore Medical, Lp Due to...

The Issue: Complaints regarding loose proximal body bolts or bolts that were found...

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

Class II — Potential Health HazardOngoing
FoodSeptember 21, 2018· Victoria Gourmet, Inc.

Recalled Item: Victoria Taylor's Seasonings - Blackening Rub Recalled by Victoria Gourmet,...

The Issue: Product labeling is incorrect.

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

Class III — Low RiskOngoing
Refund
FoodSeptember 21, 2018· Victoria Gourmet, Inc.

Recalled Item: Victoria Taylor's Seasonings - New Orleans - 5.0 oz. Recalled by Victoria...

The Issue: Product labeling is incorrect.

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

Class III — Low RiskOngoing
Refund
DrugSeptember 21, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Nystatin and Triamcinolone Acetonide Cream Recalled by Dr. Reddy's...

The Issue: Failed stability specifications - An out of specification result was...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2018· Teva Pharmaceuticals USA

Recalled Item: Clozapine Orally Disintegrating Tablets Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Disintegration Specifications: Out-of-specification disintegration...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2018· Pfizer Inc.

Recalled Item: Meropenem for Injection Recalled by Pfizer Inc. Due to Lack of assurance of...

The Issue: Lack of assurance of sterility: loss of container integrity.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 20, 2018· Pfizer Inc.

Recalled Item: Glipizide XL (glipizide) extended-release tablets 5 mg 500-tablet bottle...

The Issue: CGMP Deviations; rejected product was used to manufacture final bulk lot

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 20, 2018· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: Cardiosave Rescue IABP Recalled by Maquet Datascope Corp - Cardiac Assist...

The Issue: There is a potential for interruption and/or inability to start therapy to...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 20, 2018· AS Software, Inc.

Recalled Item: AS-OBGYN Information System version 7.824.x Recalled by AS Software, Inc....

The Issue: Any change made to current ultrasound machine software or hardware upgrades,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2018· Micro-Tech (Nanjing) Co., Ltd.

Recalled Item: Single-Use Biopsy Forceps Recalled by Micro-Tech (Nanjing) Co., Ltd. Due to...

The Issue: Single-Use Biopsy Forceps box contains incorrect product, instead it...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2018· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: Cardiosave Hybrid IABP Recalled by Maquet Datascope Corp - Cardiac Assist...

The Issue: There is a potential for interruption and/or inability to start therapy to...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: Philips DigitalDiagnost software 4.1.x and 4.2.x Recalled by Philips Medical...

The Issue: Stitching run on SkyPlate detector interrupted intermittently; Stitching...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2018· Encore Medical, Lp

Recalled Item: Flexible Drill Shaft Recalled by Encore Medical, Lp Due to Manufacturing...

The Issue: Manufacturing error, the drill bit shaft is unable to properly capture the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 19, 2018· Upsher Smith Laboratories, Inc.

Recalled Item: Bumetanide Tablets Recalled by Upsher Smith Laboratories, Inc. Due to Failed...

The Issue: Failed impurities/ degradation specifications: Product is Out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 19, 2018· Pfizer Inc.

Recalled Item: Elelyso (taliglucerase alfa) for injection Recalled by Pfizer Inc. Due to...

The Issue: Lack of assurance of sterility -Reports of loose metal ferrule crimps on...

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

Class II — Potential Health HazardOngoing
Refund