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. 2,510 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,510 in last 12 months

Showing 1288112900 of 13,369 recalls

DrugDecember 7, 2012· West-ward Pharmaceutical Corp.

Recalled Item: Propylthiouracil Tablets Recalled by West-ward Pharmaceutical Corp. Due to...

The Issue: Presence of Foreign Substance: Uncharacteristic spots identified as steel...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2012· West-ward Pharmaceutical Corp.

Recalled Item: Lisinopril Tablets Recalled by West-ward Pharmaceutical Corp. Due to...

The Issue: Presence of Foreign Substance: Uncharacteristic black spots identified as a...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2012· West-ward Pharmaceutical Corp.

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

The Issue: Presence of Foreign Substance: Uncharacteristic blacks spots on tablets.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2012· Bayer Healthcare, LLC

Recalled Item: Bronkaid Dual Action Formula Recalled by Bayer Healthcare, LLC Due to...

The Issue: Labeling: Label lacks warning or Rx legend; Certain information was...

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

Class III — Low RiskOngoing
Refund
DrugDecember 6, 2012· Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Recalled Item: Hydrocodone bitartrate and acetaminophen Tablets Recalled by Vintage...

The Issue: Superpotent (Multiple Ingredient) Drug: Complaint received of oversized tablets.

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 5, 2012· West-ward Pharmaceutical Corp.

Recalled Item: PredniSONE Tablets Recalled by West-ward Pharmaceutical Corp. Due to...

The Issue: Presence of Foreign Substance: A complaint was received for black specks...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 5, 2012· Teva Pharmaceuticals USA, Inc.

Recalled Item: Copaxone (glatiramer acetate injection) Recalled by Teva Pharmaceuticals...

The Issue: Presence of Foreign Substance: Product is being recalled due to receiving an...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 5, 2012· West-ward Pharmaceutical Corp.

Recalled Item: PredniSONE Tablets Recalled by West-ward Pharmaceutical Corp. Due to...

The Issue: Presence of Foreign Substance: Tablets are being recalled due to gray...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Green Valley Drugs

Recalled Item: Cyanocobalamin 1000 mcg/ml Recalled by Green Valley Drugs Due to...

The Issue: Non-Sterility: Green Valley Drugs received positive sterility results from...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 4, 2012· Abbott Laboratories

Recalled Item: Synthroid (Levothyroxine Sodium) tablets Recalled by Abbott Laboratories Due...

The Issue: Labeling: Error on Declared Strength. Product labeled to contain 150 mcg...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Johnson & Johnson

Recalled Item: Clean & Clear advantage Recalled by Johnson & Johnson Due to Superpotent...

The Issue: Superpotent (Single Ingredient Drug): salicylic acid

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

Class III — Low RiskOngoing
Refund
DrugDecember 4, 2012· Green Valley Drugs

Recalled Item: Methylprednisolone Preservative Free 40 mg/ml Injectible Suspension Recalled...

The Issue: Non-Sterility: Green Valley Drugs received positive sterility results from...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 4, 2012· Amedra Pharmaceuticals LLC

Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...

The Issue: Failed Dissolution Specifications: The affected lots may not meet the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Amedra Pharmaceuticals LLC

Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...

The Issue: Failed Dissolution Specifications: The affected lots may not meet the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Amedra Pharmaceuticals LLC

Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...

The Issue: Failed Dissolution Specifications: The affected lots may not meet the...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 30, 2012· West-ward Pharmaceutical Corp.

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

The Issue: Labeling: Not elsewhere classified: On 12/12/11, DEA published a final rule...

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

Class III — Low RiskOngoing
Refund
DrugNovember 30, 2012· West-ward Pharmaceutical Corp.

Recalled Item: Lisinopril and Hydrochlorothiazide Tablets Recalled by West-ward...

The Issue: Presence of Foreign Substance: Reports of gray smudges identified as minute...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 26, 2012· Pfizer Inc.

Recalled Item: TORISEL Kit (temsirolimus) injection Recalled by Pfizer Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility; potential that a low level of endotoxins may...

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

Class III — Low RiskOngoing
Refund
DrugNovember 21, 2012· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Fluorouracil Topical Cream USP Recalled by Taro Pharmaceuticals U.S.A., Inc....

The Issue: Product Lacks Stability: Out-of-specification (OOS) results were observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 21, 2012· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) Recalled by Hill Dermaceuticals,...

The Issue: Subpotent; 12 month stability timepoint

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

Class III — Low RiskOngoing
Refund