Product Recalls in North Dakota

Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,526 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,526 in last 12 months

Showing 1174111760 of 13,369 recalls

DrugOctober 21, 2013· Medisca Inc.

Recalled Item: Human Chorionic Gonadotropin Recalled by Medisca Inc. Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; Firm states that erroneous...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 18, 2013· Hospira Inc.

Recalled Item: Marcaine (bupivacaine HCl) injection Recalled by Hospira Inc. Due to...

The Issue: Presence of Particulate Matter: Units of this lot may have visible metal...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 16, 2013· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Ciclopirox Shampoo 1% Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...

The Issue: Subpotent. drug

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

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2013· B. Braun Medical Inc

Recalled Item: Cefepime for Injection USP and Dextrose Injection USP Recalled by B. Braun...

The Issue: Presence of Particulate Matter: The 1g Cefepime for Injection USP and...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 15, 2013· VistaPharm, Inc.

Recalled Item: Phenytoin Oral Suspension USP 125mg/5mL Recalled by VistaPharm, Inc. Due to...

The Issue: Defective Container: A lidding deformity allowed for the product to have out...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 11, 2013· Sandoz Inc

Recalled Item: Fosinopril Sodium and Hydrochlorothiazide Tablets Recalled by Sandoz Inc Due...

The Issue: Subpotent; Hydrochlorothiazide at the 9 month time point.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 11, 2013· Teva Pharmaceuticals USA

Recalled Item: Daunorubicin Hydrochloride Injection Recalled by Teva Pharmaceuticals USA...

The Issue: Presence of Precipitate; precipitation of drug product

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 11, 2013· Hospira Inc.

Recalled Item: 0.5% Bupivacaine HCl and Epinephrine 1:200 Recalled by Hospira Inc. Due to...

The Issue: Lack of assurance of sterility; equipment failure led to potential breach in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 11, 2013· Hospira Inc.

Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Visible particles embedded in the glass...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi BTrim ULTIMATE BOOST Dietary Supplement capsules Recalled by Pure...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi INSANE AMP'D Dietary Supplement capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi INSANE Bee Pollen Dietary Supplement Capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi BTrim MAX Dietary Supplement capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi AMP'D UP Advanced Weight Loss Dietary Supplement capsules Recalled...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi eXtreme ACCELERATOR Dietary Supplement Capsules Recalled by Pure...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 9, 2013· Actavis Elizabeth LLC

Recalled Item: Alprazolam Orally Disintegrating Tablets Recalled by Actavis Elizabeth LLC...

The Issue: Failed Tablet/Capsule Specifications; partial tablet erosion resulting in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2013· Sandoz, Inc

Recalled Item: Ropinirole Recalled by Sandoz, Inc Due to Cross contamination with other...

The Issue: Cross contamination with other products: Sandoz is recalling certain lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2013· B @ B Trade Inc.

Recalled Item: Lidiy capsules Dietary Supplement. Each bottle contains 30 capsules....

The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 7, 2013· Amedra Pharmaceuticals LLC

Recalled Item: Dexedrine¿ (Dextroamphetamine Sulfate) Spansules¿ Sustained Release Capsules...

The Issue: Failed Dissolution Specifications: Out of Specification (OOS) test results...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2013· B @ B Trade Inc.

Recalled Item: Slim Fortune capsules Dietary Supplement. Each bottle contains 30 capsules....

The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund