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. 2,776 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,776 in last 12 months

Showing 1428114300 of 30,153 recalls

Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet Recalled...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER Recalled by Bard Peripheral...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Bard Peripheral Vascular Inc

Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet Recalled by...

The Issue: The action is being initiated due to complaints received concerning the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Baxter Healthcare Corporation

Recalled Item: REVACLEAR 400 Dialyzer Recalled by Baxter Healthcare Corporation Due to...

The Issue: There is a potential presence of ruptured dialyzer fibers which may lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Baxter Healthcare Corporation

Recalled Item: REVACLEAR 300 Dialyzer Recalled by Baxter Healthcare Corporation Due to...

The Issue: There is a potential presence of ruptured dialyzer fibers which may lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2019· Infinium Medical, Inc

Recalled Item: CLEO Patient Monitor /Tranquility VS Patient Monitor Recalled by Infinium...

The Issue: The CLEO & Tranquility VS Patient Monitors 510(k) indications for use in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Boston Scientific Neuromodulation Corporation

Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...

The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Boston Scientific Neuromodulation Corporation

Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...

The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Boston Scientific Neuromodulation Corporation

Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...

The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Boston Scientific Neuromodulation Corporation

Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...

The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Boston Scientific Neuromodulation Corporation

Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...

The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Paltop Advanced Dental Solutions Ltd

Recalled Item: Paltop Advanced Plus Dental Implant Dia 6.0mm L10mm Catalog Number:...

The Issue: Surface micro/nano topography on some of the implants contained within this...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Becton Dickinson & Company

Recalled Item: BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part Number:...

The Issue: Lot has been confirmed to have no additive within the tube. Sample processed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Medline Industries, Inc.

Recalled Item: Anti-fog solution packaged in a Tyvek peel pouch and it Recalled by Medline...

The Issue: The Anti-Fog Solution may not defog properly due to a degradation in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2019· Spectrum Medical Ltd.

Recalled Item: Quantum Pump Console Recalled by Spectrum Medical Ltd. Due to Potential for...

The Issue: Potential for Quantum Pump Console, part of the Quantum Perfusion Systems,...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 29, 2019· Pega Medical Inc.

Recalled Item: SLIM Handle - catalogue #: SLM-HND100 a component of Simple Recalled by Pega...

The Issue: Handle could jam with the Driver due to the detachment of an internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2019· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Liberty Cycler Cassettes (a disposable cassette that is intended to Recalled...

The Issue: Additional Instructions: step-by step handling and inserting the cassette...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2019· Siemens Healthcare Diagnostics Inc

Recalled Item: Stratus CS Acute Care cTNI TestPak Recalled by Siemens Healthcare...

The Issue: Potential for increased rate of false positive results and/or increased rate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2019· AtriCure, Inc.

Recalled Item: EPi-Sense Guided Coagulation System with Visitrax Recalled by AtriCure, Inc....

The Issue: The sterile package seal for the Epi-Sense Guided Coagulation System may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Nobel Biocare Usa Llc

Recalled Item: Healing Abutment Conical Connection RP 0 3.6 x 5mm Recalled by Nobel Biocare...

The Issue: Packaged dental implant healing abutments were found to contain the wrong...

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

Class II — Potential Health HazardOngoing