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. 2,656 recalls have been distributed to New York in the last 12 months.
Showing 29541–29560 of 55,896 recalls
Recalled Item: Discovery IGS 730 Interventional Fluoroscopic X-ray Systems Recalled by GE...
The Issue: The Discovery IGS and Innova IGS systems may experience X-ray abort errors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova IGS 630/520/530/540 Interventional Fluoroscopic X-ray Systems...
The Issue: The Discovery IGS and Innova IGS systems may experience X-ray abort errors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...
The Issue: Cap-adapter assembly of the device may potentially not be adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...
The Issue: Cap-adapter assembly of the device may potentially not be adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...
The Issue: Cap-adapter assembly of the device may potentially not be adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...
The Issue: Cap-adapter assembly of the device may potentially not be adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...
The Issue: Cap-adapter assembly of the device may potentially not be adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental System Proximal Femoral Component 38mm Offset Recalled by...
The Issue: There is a potential for debris in the hole on the superior lateral aspect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...
The Issue: The dose calculation accuracy may in some situations be less than expected....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Acute Care System (lACS) Monitoring Solution Recalled by Draegar...
The Issue: Software anomaly resulting in the loss of patient settings and stored...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Molleave Recalled by Elroselabs Inc. Due to cGMP Deviations
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Conzerol zero molluscum contagiosum Recalled by Elroselabs Inc. Due to cGMP...
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Conzerol (antipoxin) H2O2 Gel Recalled by Elroselabs Inc. Due to cGMP Deviations
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.