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. 2,840 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,840 in last 12 months

Showing 96019620 of 13,591 recalls

DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: L-Glutamine Injectable Recalled by Downing Labs, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: Magnesium Sulfate Injection (4060mOsm/L) Recalled by Downing Labs, LLC Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: L-Tryptophan Injectable Recalled by Downing Labs, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: M.I.C Injection (Preserved) Recalled by Downing Labs, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: EDTA Disodium Injectable Recalled by Downing Labs, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: Magnesium Sulfate Injectable Recalled by Downing Labs, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: Taurine Injectable Recalled by Downing Labs, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 16, 2015· Downing Labs, LLC

Recalled Item: Thiotic Acid Injection Recalled by Downing Labs, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 13, 2015· Rx PAK

Recalled Item: Donnatal (Phenobarbital Recalled by Rx PAK Due to Labeling: Not elsewhere...

The Issue: Labeling: Not elsewhere classified - Product label incorrectly lists...

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

Class III — Low RiskOngoing
Refund
DrugOctober 9, 2015· Qualgen

Recalled Item: Estradiol USP 99.5% Recalled by Qualgen Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: The firm is recalling all sterile...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2015· Qualgen

Recalled Item: Testosterone USP 99.5% Recalled by Qualgen Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: The firm is recalling all sterile...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2015· Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Recalled Item: HYDROCHLOROTHIAZIDE CAPSULES Recalled by Vintage Pharmaceuticals LLC, DBA...

The Issue: Presence of Particulate Matter.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2015· Inaffit, LLC

Recalled Item: NATUREAL BURN FAT NATURE Recalled by Inaffit, LLC Due to Undeclared Sibutramine

The Issue: Marketed Without an Approved NDA/ANDA: Product contains undeclared sibutramine.

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 1, 2015· MSNV, Inc dba National Video Supply

Recalled Item: Rhino 7 3000 Recalled by MSNV, Inc dba National Video Supply Due to...

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 1, 2015· Tribute Pharmaceuticals US Inc.

Recalled Item: Fenofibric Acid Tablets Recalled by Tribute Pharmaceuticals US Inc. Due to...

The Issue: Chemical Contamination: The product may contain trace amounts of...

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

Class III — Low RiskOngoing
Refund
DrugOctober 1, 2015· Tribute Pharmaceuticals US Inc.

Recalled Item: Fenofibric Acid Tablets 105 mg Recalled by Tribute Pharmaceuticals US Inc....

The Issue: Chemical Contamination: The product may contain trace amounts of...

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

Class III — Low RiskOngoing
Refund
DrugOctober 1, 2015· MSNV, Inc dba National Video Supply

Recalled Item: Rhino 7 Platinum 3000 Recalled by MSNV, Inc dba National Video Supply Due to...

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 30, 2015· Premiere Sales Group

Recalled Item: Rhino 7 3000 Recalled by Premiere Sales Group Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 30, 2015· Premiere Sales Group

Recalled Item: Rhino 7 Platinum 3000 Recalled by Premiere Sales Group Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 29, 2015· Fit Firm and Fabulous

Recalled Item: Ultimate Herbal Slimcap Capsules Recalled by Fit Firm and Fabulous Due to...

The Issue: Marketed Without An Approved NDA/ANDA: product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund