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.
Showing 12601–12620 of 55,896 recalls
Recalled Item: Disposable Surgical Level 3 Gown Recalled by Texas Medical Technology Inc....
The Issue: Surgical gowns recalled due to gown fabric failing to pass the hydrostatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Introcan Safety FEP 14G Recalled by B Braun Medical Inc Due to Potential for...
The Issue: Potential for leakage at the catheter hub.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veritas Advanced Infusion Packs. Used in ophthalmic procedures. Recalled by...
The Issue: As a result of returned product complaints for Veritas Phaco packs related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine Hydrochloride Jelly USP Recalled by Akorn, Inc. Due to cGMP...
The Issue: cGMP Deviations: Turbidity discovered in Artificial Tears Ointment during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Chloride Ophthalmic Ointment USP Recalled by Akorn, Inc. Due to cGMP...
The Issue: cGMP Deviations: Turbidity discovered in Artificial Tears Ointment during...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FULL VISION INC. TRACKMASTER Recalled by Full Vision Inc Due to This has...
The Issue: This has been identified a rare occurrence, under a specific scenario, where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FULL VISION INC. TRACKMASTER Recalled by Full Vision Inc Due to This has...
The Issue: This has been identified a rare occurrence, under a specific scenario, where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FULL VISION INC. TRACKMASTER Recalled by Full Vision Inc Due to This has...
The Issue: This has been identified a rare occurrence, under a specific scenario, where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FULL VISION INC. TRACKMASTER Recalled by Full Vision Inc Due to This has...
The Issue: This has been identified a rare occurrence, under a specific scenario, where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FULL VISION INC. TRACKMASTER Recalled by Full Vision Inc Due to This has...
The Issue: This has been identified a rare occurrence, under a specific scenario, where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FULL VISION INC. TRACKMASTER Recalled by Full Vision Inc Due to This has...
The Issue: This has been identified a rare occurrence, under a specific scenario, where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FULL VISION INC. TRACKMASTER Recalled by Full Vision Inc Due to This has...
The Issue: This has been identified a rare occurrence, under a specific scenario, where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-X ROVER MOBILE X-RAY SYSTEM Recalled by Micro-X Ltd. Due to Software...
The Issue: Software calibration error with product equip with a Dose Area Product (DAP)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains...
The Issue: Excessive ultraviolet-C radiation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N Antiserum to Human IgG Recalled by SIEMENS HEALTHCARE DIAGNOSTICS INC Due...
The Issue: N Antiserum to Human IgG are not meeting the current High-Dose Hook Effect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N Antiserum to Human IgG Recalled by SIEMENS HEALTHCARE DIAGNOSTICS INC Due...
The Issue: N Antiserum to Human IgG are not meeting the current High-Dose Hook Effect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hammertoe Continuous Compression Implant (CCI) Kit Part Number: 46.239.001...
The Issue: Drill Pin (drill bit) is not compatible with the Drill Template included in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle3 Radiation Therapy Planning System Recalled by Philips Medical...
The Issue: When computing a radiation dose in the system, the exported dose information...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Inc Due to...
The Issue: Labeling: Label Error on Declared Strength; A sealed 100-count bottle...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Haiyue Food Nutritional Preserved Vegetable Recalled by XIUMIN LIN Due to...
The Issue: Contains Cyclamate
Recommended Action: Do not consume. Return to store for a refund or discard.