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. 2,632 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,632 in last 12 months

Showing 3390133920 of 55,896 recalls

DrugApril 6, 2017· Isomeric Pharmacy Solution, LLC

Recalled Item: Methylprednisolone Acetate 80 mg/mL Recalled by Isomeric Pharmacy Solution,...

The Issue: Lack of Assurance of Sterility: due to concerns with production processes...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 6, 2017· Seafarers Inc.

Recalled Item: Pre-cooked Recalled by Seafarers Inc. Due to Potential Listeria Contamination

The Issue: Products may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2017· Seafarers Inc.

Recalled Item: Pre-cooked Recalled by Seafarers Inc. Due to Potential Listeria Contamination

The Issue: Products may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 6, 2017· Seafarers Inc.

Recalled Item: Precooked Recalled by Seafarers Inc. Due to Potential Listeria Contamination

The Issue: Products may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 6, 2017· Merge Healthcare, Inc.

Recalled Item: Fellows "Mighty 8" Power strip (Part Number 04175-0008) and TrippLite...

The Issue: Merge is conducting a hardware recall (replacement) of Fellows "Mighty 8"...

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

Class II — Potential Health HazardOngoing
FoodApril 5, 2017· Oberlander Baking Co

Recalled Item: Oberlander Bakery Gluten Free Brand Chocolate Kokosh Cake Net Wt. Recalled...

The Issue: Oberlander Gluten Free Brand Chocolate Kokosh Cake chocolate filled cake...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 5, 2017· Bausch & Lomb Surgical, Inc.

Recalled Item: SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for Recalled...

The Issue: Complaints concerning kinked haptics that were occurring during lens delivery.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2017· Boston Scientific Corporation

Recalled Item: The JETSTREAM is a rotational atherectomy catheter system designed for...

The Issue: Boston Scientific is initiating a voluntary removal of two lots of JETSTREAM...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2017· Diagnostic Hybrids, Inc.

Recalled Item: MicroVue CIC-C1q EIA Recalled by Diagnostic Hybrids, Inc. Due to There is a...

The Issue: There is a potential for the slope of the standard curve to fail to meet the...

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

Class II — Potential Health HazardOngoing
DrugApril 3, 2017· Cell Distributors

Recalled Item: Tears (Carboxymethylcellulose Sodium Solution) 0.5% Recalled by Cell...

The Issue: Labeling: Not elsewhere classified; product labeling lacks a NDC number, net...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2017· Medisca, Inc.

Recalled Item: ESTRADIOL Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...

The Issue: cGMP Deviations; manufacturer initiated recall of API product after...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2017· Medisca, Inc.

Recalled Item: ESTRONE Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...

The Issue: cGMP Deviations; manufacturer initiated recall of API product after...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2017· Medisca, Inc.

Recalled Item: ESTRADIOL Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...

The Issue: cGMP Deviations; manufacturer initiated recall of API product after...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2017· Medisca, Inc.

Recalled Item: ESTRIOL Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...

The Issue: cGMP Deviations; manufacturer initiated recall of API product after...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 3, 2017· Intersurgical Inc

Recalled Item: Solus Flexible wire-reinforced laryngeal mask airways under the following...

The Issue: A defect in the wire-reinforced tubing may result in a partial of total...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2017· Mederi Therapeutics, Inc

Recalled Item: Mederi Stretta Catheter and Accessory Kit Recalled by Mederi Therapeutics,...

The Issue: Product sterility compromised due to breach in sterile barrier package

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2017· Natus Medical Incorporated

Recalled Item: Second generation neoBLUE LED Phototherapy Light (neoBLUE 2) sold between...

The Issue: The second generation neoBLUE 2 lights with a black band, sold from 2003 to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2017· Beckman Coulter Inc.

Recalled Item: AQUIOS CL Flow Cytometer Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter has confirmed that the Export feature located in the Results...

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

Class II — Potential Health HazardOngoing
FoodApril 1, 2017· Killer Brownie Distributing LLC

Recalled Item: ORIGINAL KB KILLER BROWNIE¿ 3x35 CT NET WT 36 LBS (16.33 kg) CONTAINS: Milk...

The Issue: The firm was notified by a customer that they received product that was...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 1, 2017· Killer Brownie Distributing LLC

Recalled Item: GERMAN CHOCOLATE KB KILLER BROWNIE¿ 3x35 CT NET WT 36 Recalled by Killer...

The Issue: The firm was notified by a customer that they received product that was...

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

Class I — Serious Health HazardOngoing
Refund