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. 2,837 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,837 in last 12 months

Showing 97219740 of 30,153 recalls

Medical DeviceJuly 6, 2021· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM BR 27.29 (BR) Assay 250 Test Kit ()- Recalled by Siemens...

The Issue: Product does not meet the Instructions for Use (IFU) claimed Pack...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2021· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM BR 27.29 (BR) Assay 250 Test Kit- in Recalled by Siemens...

The Issue: Product does not meet the Instructions for Use (IFU) claimed Pack...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2021· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM BR 27.29 (BR) Assay 50 Test Kit- in Recalled by Siemens...

The Issue: Product does not meet the Instructions for Use (IFU) claimed Pack...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2021· Advance Dx, Inc.

Recalled Item: Advance Dx 100 Blood Collection Card Quantity 25 Recalled by Advance Dx,...

The Issue: Due to high glucose test results when using the blood collection cards.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2021· Zeltiq Aesthetics, Inc

Recalled Item: CoolSculpting Elite System The CoolSculpting System SW release 2.0 Recalled...

The Issue: An incorrect error messaging system that could potentially lead to: 1)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2021· Laboratoires Bodycad, Inc.

Recalled Item: Torque Limiting Adaptor Recalled by Laboratoires Bodycad, Inc. Due to There...

The Issue: There is a risk of breakage of the torque limiting adaptor if used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2021· Hero Health

Recalled Item: The Hero Model 100 (H-100) is a system consisting of Recalled by Hero Health...

The Issue: Due to dispenser prompting for a missed dose that had already been dispensed

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Gibson Bioscience

Recalled Item: Potassium Hydroxide 10% (KOH 10%) Recalled by Gibson Bioscience Due to A lot...

The Issue: A lot of KOH 10% was made with Hydrogen Peroxide 3% instead of KOH 10%.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Howmedica Osteonics Corp.

Recalled Item: Triathlon Prim CEM FXD BPLT 7 Recalled by Howmedica Osteonics Corp. Due to...

The Issue: The internal profile of the Triathlon Prim (Baseplate) is potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Medline Industries Inc

Recalled Item: Medline Arthroscopy Kit Recalled by Medline Industries Inc Due to The kits...

The Issue: The kits may contain an expired component.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Beckman Coulter Inc.

Recalled Item: ACCESS SARS-CoV-2 ANTIGEN QC Recalled by Beckman Coulter Inc. Due to...

The Issue: SARS-CoV-2 Antigen Assay test may generate false positive results which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Beckman Coulter Inc.

Recalled Item: ACCESS SARS-CoV-2 ANTIGEN EXTRACTION SOLUTION Recalled by Beckman Coulter...

The Issue: SARS-CoV-2 Antigen Assay test may generate false positive results which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Medline Industries Inc

Recalled Item: Medline Knee Arthroscopy Kit Recalled by Medline Industries Inc Due to The...

The Issue: The kits may contain an expired component.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Beckman Coulter Inc.

Recalled Item: ACCESS SARS-CoV-2 Antigen Recalled by Beckman Coulter Inc. Due to SARS-CoV-2...

The Issue: SARS-CoV-2 Antigen Assay test may generate false positive results which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Medline Industries Inc

Recalled Item: Medline Total Knee Recalled by Medline Industries Inc Due to The kits may...

The Issue: The kits may contain an expired component.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Medline Industries Inc

Recalled Item: Medline Shoulder CDS convenience kits Recalled by Medline Industries Inc Due...

The Issue: The kits may contain an expired component.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Beckman Coulter Inc.

Recalled Item: Access SARS-CoV-2 Antigen Calibrators Recalled by Beckman Coulter Inc. Due...

The Issue: SARS-CoV-2 Antigen Assay test may generate false positive results which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2021· Verathon, Inc.

Recalled Item: GlideScope Go Monitors Recalled by Verathon, Inc. Due to Handheld video...

The Issue: Handheld video monitor failed to meet the labeled IP67 rating which may...

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

Class III — Low RiskOngoing
Medical DeviceJune 30, 2021· GE Healthcare, LLC

Recalled Item: Revolution Apex Recalled by GE Healthcare, LLC Due to The accumulated dose...

The Issue: The accumulated dose is incorrectly displayed in certain situations. There...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2021· GE Healthcare, LLC

Recalled Item: Revolution CT Recalled by GE Healthcare, LLC Due to The accumulated dose is...

The Issue: The accumulated dose is incorrectly displayed in certain situations. There...

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

Class II — Potential Health HazardOngoing