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. 1,215 recalls have been distributed to New York in the last 12 months.
Showing 2041–2060 of 55,896 recalls
Recalled Item: YoCrunch Low Fat Yogurt with Toppers Recalled by DANONE US LLC Due to...
The Issue: Foreign material (plastic pieces)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Blood/EMB Recalled by Remel, Inc Due to Potential Listeria Contamination
The Issue: The products may contain surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YoCrunch Lowfat Yogurt with Toppers Recalled by DANONE US LLC Due to Foreign...
The Issue: Foreign material (plastic pieces)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: YoCrunch Low Fat Yogurt with Toppers Recalled by DANONE US LLC Due to...
The Issue: Foreign material (plastic pieces)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BritePro Solo Single-Use Fiber Optic Laryngoscope Handle :040-310AU and...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handle Recalled by...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Agar Recalled by Remel, Inc Due to Potential Listeria Contamination
The Issue: The products may contain surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood/MacConkey Biplate 100/PK Recalled by Remel, Inc Due to Potential...
The Issue: The products may contain surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM Recalled by Onkos Surgical, Inc. Due to...
The Issue: Unidentified substance of unknown impact was identified on devices during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handle Recalled by...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sucralfate Tablets Recalled by Nostrum Laboratories, Inc. Due to CGMP...
The Issue: CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024....
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BritePro Solo Single-Use Fiber Optic Handle and Blade : 040-331U (Mac 1)...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Joystick R-net. Electrical wheelchair component. Recalled by mo-Vis...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray NGDS Warrior Panel NGDS-ASY-0007 is a qualitative Recalled by...
The Issue: FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Thyroglobulin assay Recalled by Beckman Coulter, Inc. Due to Access...
The Issue: Access Thyroglobulin reagent lot 439163 may generate erroneously high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDM-ARLITE-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bicillin L-A (penicillin G benzathine injectable suspension) Recalled by...
The Issue: CGMP Deviations; particulates identified during visual inspection
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IDM-MICRO-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due to...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDM-MULTI-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due to...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.