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. 2,846 recalls have been distributed to New York in the last 12 months.
Showing 7861–7880 of 30,153 recalls
Recalled Item: Recreo Hair Growth Laser Comb Recalled by OMM Imports, Inc. dba Zero Gravity...
The Issue: The firm distributed the laser products without affixing the warning,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: 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: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...
The Issue: Incidents of device splitting or detaching during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.