Product Recalls in Vermont

Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,499 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,499 in last 12 months

Showing 94219440 of 13,356 recalls

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 16, 2015· Downing Labs, LLC

Recalled Item: L-Glutathione 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 16, 2015· Downing Labs, LLC

Recalled Item: Magnesium Chloride Hexahydrate Injection 200mg/mL Recalled by Downing Labs,...

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-Tyrosine Injectable Recalled by Downing Labs, LLC Due to Lack of Assurance...

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: MIC w/Methyl B-12 Preserved Injection Recalled by Downing Labs, LLC Due to...

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: 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 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 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· 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· 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 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 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 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 29, 2015· Hospira Inc.

Recalled Item: Amidate (Etomidate Injection Recalled by Hospira Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification(OOS)...

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

Class III — Low RiskOngoing
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
DrugSeptember 28, 2015· Perrigo Company PLC

Recalled Item: Cetirizine HCl 10 mg Tablet Recalled by Perrigo Company PLC Due to Failed...

The Issue: Failed Impurity/Degradations Specifications; impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2015· Medline Industries Inc

Recalled Item: ACETAMINOPHEN REGULAR-STRENGTH PAIN RELIEVER tablets Recalled by Medline...

The Issue: Labeling: Label Error on Declared Strength- Bottles containing 500 mg...

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

Class I — Serious Health HazardOngoing
Refund