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 1010110120 of 30,153 recalls

Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2021· Alphatec Spine, Inc.

Recalled Item: Atec Insignia Anterior Cervical Plate System Recalled by Alphatec Spine,...

The Issue: There is a potential for the screw blocking mechanism on the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2021· LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD

Recalled Item: Leccurate SARS-CoV-2 Recalled by LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD...

The Issue: Leccurate SARS-CoV-2, Antibody Rapid Test Kit (Colloidal Gold...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 26, 2021· Roche Diagnostics Operations, Inc.

Recalled Item: IRON GEN 2: ROCHE COBAS INTEGRA ANALYZER Recalled by Roche Diagnostics...

The Issue: Roche received several complaints regarding increased control recovery and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2021· Synaptive Medical Inc

Recalled Item: Synaptive Trackable Suction Set Standard and Malleable Recalled by Synaptive...

The Issue: Due to visible burrs/metal filings affixed along the suction tube inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2021· Philips North America Llc

Recalled Item: Ingenia Ambition X - Model Number: 781356 Recalled by Philips North America...

The Issue: The MR magnet is equipped with 4 lifting blocks, which are positioned on top...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2021· Philips North America Llc

Recalled Item: Ingenia Ambition S - Model Number: 781359 Diagnostic MR system. Recalled by...

The Issue: The MR magnet is equipped with 4 lifting blocks, which are positioned on top...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2021· Welch Allyn Inc

Recalled Item: GS777 Wall Transformer Model: 77710 Intended Use: The GS777 Wall Recalled by...

The Issue: Potential Risk of fluid ingress to the power supplies, resulting in risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2021· Welch Allyn Inc

Recalled Item: ProBP 3400 Digital Blood Pressure Device ((handheld Recalled by Welch Allyn...

The Issue: Potential Risk of fluid ingress to the power supplies, resulting in risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2021· Remel Inc

Recalled Item: Remel Bile Esculin Azide Agar w/ 6mcg/ml Vancomycin Recalled by Remel Inc...

The Issue: The media allows growth of E. faecalis ATCC 29212 with blackening of the media.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2021· Potomac River Group, Corp.

Recalled Item: RAPTAR Laser Range Finders Recalled by Potomac River Group, Corp. Due to...

The Issue: RAPTAR units are capable of being field modified to enable the use of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2021· INNOVATIVE TOMOGRAPHY PRODUCT GMBH

Recalled Item: Semi-automatic Biopsy-Needle Recalled by INNOVATIVE TOMOGRAPHY PRODUCT GMBH...

The Issue: Sterility Assurance; Coaxial Interventional Needle labeled as sterile may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2021· INNOVATIVE TOMOGRAPHY PRODUCT GMBH

Recalled Item: Coaxial Interventional Needle Recalled by INNOVATIVE TOMOGRAPHY PRODUCT GMBH...

The Issue: Sterility Assurance; Coaxial Interventional Needle labeled as sterile may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2021· INNOVATIVE TOMOGRAPHY PRODUCT GMBH

Recalled Item: Coaxial Interventional Needle Recalled by INNOVATIVE TOMOGRAPHY PRODUCT GMBH...

The Issue: Sterility Assurance; Coaxial Interventional Needle labeled as sterile may...

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

Class II — Potential Health HazardOngoing