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. 2,603 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,603 in last 12 months

Showing 3864138660 of 55,896 recalls

Medical DeviceMarch 25, 2016· Monteris Medical Corp

Recalled Item: NeuroBlate System SideFire Select 2.2 mm Directional Laser Probe Recalled by...

The Issue: Monteris received a report that the sapphire lens on a 2.2SF probe fractured...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2016· Becton Dickinson & Company

Recalled Item: Henry Schein Single Use Syringe Luer-Lock Recalled by Becton Dickinson &...

The Issue: BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2016· Becton Dickinson & Company

Recalled Item: Henry Schein Single Use Syringe Luer-Lock Recalled by Becton Dickinson &...

The Issue: BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm...

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

Class II — Potential Health HazardOngoing
FoodMarch 25, 2016· Ryszard Food Distributor, Inc.

Recalled Item: Novus Snack brand Golden Raisins Recalled by Ryszard Food Distributor, Inc....

The Issue: The product contained undeclared sulfites (1337.2 ppm) based on sampling and...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 25, 2016· Strong America Limited

Recalled Item: Welltop Fried Dace Recalled by Strong America Limited Due to FDA sampling...

The Issue: FDA sampling discovered the presence of leucomalachite green

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

Class III — Low RiskOngoing
Refund
DrugMarch 25, 2016· Bryant Ranch Prepack Inc.

Recalled Item: Venlafaxine 75 mg Tablet Recalled by Bryant Ranch Prepack Inc. Due to...

The Issue: Labeling: Label Mix-Up: Bryant Ranch received Tevas venlafaxine...

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

Class III — Low RiskOngoing
Refund
DrugMarch 25, 2016· B. Braun Medical Inc

Recalled Item: 5% Dextrose Injection USP Recalled by B. Braun Medical Inc Due to...

The Issue: Non-Sterility: fungal contamination due to leaking containers.

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 24, 2016· Lupin Limited

Recalled Item: Escitalopram Tablets USP 20 mg Recalled by Lupin Limited Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Expiration Date

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

Class III — Low RiskOngoing
Refund
DrugMarch 24, 2016· AbbVie Inc.

Recalled Item: Zemplar (paricalcitol) capsules Recalled by AbbVie Inc. Due to Failed...

The Issue: Failed Content Uniformity Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance BigBore Oncology Computed Tomography X-ray systems Recalled by...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Siemens Healthcare Diagnostics Inc.

Recalled Item: Dimension Vista 1500 Intelligent Lab System running on software versions...

The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray systems is intended to produce...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT 16 Power Computed Tomography X-ray systems is intended...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Computed Tomography X-ray systems is intended to produce...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Siemens Healthcare Diagnostics Inc.

Recalled Item: Dimension Vista 500 Intelligent Lab System running on software versions...

The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance BigBore Radiology Computed Tomography X-ray systems Recalled by...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 Computed Tomography X-ray systems is intended to Recalled...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Teleflex Medical

Recalled Item: Weck EFx Classic Fascial Closure System Recalled by Teleflex Medical Due to...

The Issue: Incorrect expiration date was printed on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 16 Computed Tomography X-ray systems is intended to produce...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Abbott Laboratories

Recalled Item: The ARCHITECT Estradiol Kit Intended to measure estradiol Recalled by Abbott...

The Issue: Interaction of Fulvestrant with the ARCHITECT Estradiol assay, leading to...

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

Class II — Potential Health HazardOngoing