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 7281–7300 of 55,896 recalls
Recalled Item: Omeza Skin Protectant Recalled by OMEZA LLC Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Omeza Lidocaine Lavage pain relief oil 10*2mL VIALS Recalled by OMEZA LLC...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TrueDent Clear Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueDent Yellow Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueDent Cyan Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueDent Magenta Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueDent White Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INS5HND / Integra Cranial access kit (without Prep Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : HITHSP04 / Integra Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INS7260 / Integra¿ Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INS7270 / Integra¿ Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INS7250 / Integra Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : 31156 / COMBO KIT CONTAINS INS-8301 Recalled by Integra LifeSciences Corp....
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INS7280 / Integra¿ Cranial Access Kit. For access to the Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INSHITHND / Integra¿ Cranial access kit (without Prep Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : HITHSP06 / Integra Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INSHITH / Integra¿ Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INSHITHRZN / Integra Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE VIABIL Short Wire Biliary Endoprosthesis Recalled by W.L. Gore &...
The Issue: Devices without transmural drainage holes may be mislabeled as devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Whitley's Peanut Factory Recalled by Whitley Peanut Factory, Inc. Due to...
The Issue: Undeclared Allergen (peanuts, milk, soy, wheat, and sesame).
Recommended Action: Do not consume. Return to store for a refund or discard.