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. 971 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
971 in last 12 months

Showing 48381–48400 of 55,896 recalls

DrugMarch 4, 2014· Sagent Pharmaceuticals Inc

Recalled Item: Zoledronic Acid Injection 5 mg per 100 mL (0.05 mg/mL) Recalled by Sagent...

The Issue: Lack of Assurance of Sterility; leaking of premix bags

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

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

Recalled Item: Syphilis 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: EDDP 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: Oxycodone 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: CK-MB 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: Syphilis Test Card Whole Blood(Serum) LumiQuick Recalled by LumiQuick...

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: Barbiturate 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: Drugs of Abuse Panel Test Device Recalled by LumiQuick Diagnostics Inc. Due...

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: Cocaine Strip 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· LumiQuick Diagnostics Inc.

Recalled Item: Ketamine 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: Morphine Test Card (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
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Morphine Strip (300) 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: Tramadol 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: Myoglobin 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: Salmonella typhi Antigen Test Card 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: Amphetamine 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: Buprenorphine Test Strip 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: Alcohol Test 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· LumiQuick Diagnostics Inc.

Recalled Item: Dengue IgG/IgM 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: H. Pylori Ab 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