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. 2,659 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,659 in last 12 months

Showing 2620126220 of 30,153 recalls

Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: CK-MB Test Card (serum) Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: PSA Test Card (Whole Blood) Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Amphetamine Test Card Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Clonazepam Test Card Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Ketamine Test Card Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Tuberculosis Antibody Test Card Serum Recalled by LumiQuick Diagnostics Inc....

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: MDMA/Ecstasy Test Card Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Fentanyl Test Card Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Strep A Test Card Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Morphine Test Card (300) Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: PSA Test Card (Serum) Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Legionella Test Card Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: THC Test Card Recalled by LumiQuick Diagnostics Inc. Due to Products shipped...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· Teleflex Medical

Recalled Item: Sengstaken Tube and Sengstaken-Blakemore Tube. Teleflex product codes 204800...

The Issue: Sterility of the product cannot be guaranteed.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Methadone Test Card Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Methylphenidate Test Card Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Malaria pan Antigen Test Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Fentanyl Test Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Fentanyl Test Card Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Morphine Strips (2000) Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing