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 1170111720 of 13,369 recalls

DrugNovember 21, 2013· B. Braun Medical Inc

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

The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 21, 2013· B. Braun Medical Inc

Recalled Item: TrophAmine (10% Amino Acid Injection) Recalled by B. Braun Medical Inc Due...

The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 19, 2013· Vitality Research Labs LLC

Recalled Item: vitaliKOR Ready When You Are Recalled by Vitality Research Labs LLC Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling found undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 19, 2013· Tendex

Recalled Item: P-BOOST Capsules Dietary Supplement 500 mg Recalled by Tendex Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 19, 2013· Tendex

Recalled Item: NATURECT Capsules Dietary Supplement 500 mg Recalled by Tendex Due to...

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 18, 2013· Fossil Fuel Products, LLC

Recalled Item: RezzRX capsules Recalled by Fossil Fuel Products, LLC Due to Undeclared...

The Issue: Marketed Without an Approved NDA/ANDA: Fossil Fuel Products, is recalling...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 18, 2013· Baxter Healthcare Corp.

Recalled Item: 50 mg Nitroglycerin in 5% Dextrose Injection (200 mcg/mL) Recalled by Baxter...

The Issue: Presence of Particulate Matter; particulate matter in one vial identified as...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 18, 2013· Baxter Healthcare Corp.

Recalled Item: Clinimix 5/15 sulfite-free (5% Amino Acid in 15% Dextrose) Injection...

The Issue: Presence of Particulate Matter: Particulate matter includes wood, sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 18, 2013· Baxter Healthcare Corp.

Recalled Item: Clinimix E 4.25/10 sulfite-free (4.25% Amino Acid with Electrolytes in...

The Issue: Presence of Particulate Matter: Particulate matter includes wood, sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 18, 2013· Baxter Healthcare Corp.

Recalled Item: Clinimix 4.25/25 sulfite-free (4.25% Amino Acid in 25% Dextrose) Injection...

The Issue: Presence of Particulate Matter: Particulate matter includes wood, sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 18, 2013· Fougera Pharmaceuticals Inc.

Recalled Item: KETOCONAZOLE CREAM Recalled by Fougera Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-Specification degradant...

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2013· Actavis Inc

Recalled Item: BuPROPion Hydrochloride Extended-Release Tablet (XL) 150mg Recalled by...

The Issue: Failed Dissolution Specifications: Failed stability testing for dissolution...

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

Class III — Low RiskOngoing
Refund
DrugNovember 14, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Fluconazole Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc. Due...

The Issue: Failed Stability Specifications: this product is below specification for...

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

Class III — Low RiskOngoing
Refund
DrugNovember 13, 2013· Forest Pharmaceuticals Inc

Recalled Item: Namenda XR (memantine HCl) Recalled by Forest Pharmaceuticals Inc Due to...

The Issue: Failed Dissolution Specifications: Three lots of product being recalled...

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

Class III — Low RiskOngoing
Refund
DrugNovember 13, 2013· Forest Pharmaceuticals Inc

Recalled Item: Namenda XR (memantine HCl) Recalled by Forest Pharmaceuticals Inc Due to...

The Issue: Failed Dissolution Specifications: Three lots of product being recalled...

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

Class III — Low RiskOngoing
Refund
DrugNovember 13, 2013· Forest Pharmaceuticals Inc

Recalled Item: Namenda XR (memantine HCl) Recalled by Forest Pharmaceuticals Inc Due to...

The Issue: Failed Dissolution Specifications: Three lots of product being recalled...

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2013· Baxter Healthcare Corp.

Recalled Item: 10% Recalled by Baxter Healthcare Corp. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility; Drug product leaking from container...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Valacyclovir Hydrochloride Tablets Recalled by Teva Pharmaceuticals USA,...

The Issue: Presence of Foreign Tablets/Capsules: Potential of Pravastatin tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2013· Fresenius Kabi USA, LLC

Recalled Item: PACLITAXEL INJECTION Recalled by Fresenius Kabi USA, LLC Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Package Insert- Missing text on the product...

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

Class III — Low RiskOngoing
Refund
DrugNovember 7, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: Carisoprodol Tablets Recalled by West-Ward Pharmaceutical Corp. Due to...

The Issue: Presence of Foreign Substance; heavy metals (chromium, titanium etc) and...

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

Class II — Potential Health HazardOngoing
Refund