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 1176111780 of 13,369 recalls

DrugOctober 7, 2013· B @ B Trade Inc.

Recalled Item: Slim Expert softgel capsules Dietary Supplement. One month supply/ 30...

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 2, 2013· Nephron Pharmaceuticals Corp.

Recalled Item: Albuterol Sulfate Inhalation Solution Recalled by Nephron Pharmaceuticals...

The Issue: Lack of Assurance of Sterility: Nephron Pharmaceuticals Corporation...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2013· G & W Laboratories Inc

Recalled Item: G & W Fluocinolone Acetonide Cream USP 0.025% Recalled by G & W Laboratories...

The Issue: Failed Content Uniformity Specifications; at the 18 month time point.

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2013· Haute Health, LLC

Recalled Item: PHUK Sexual Enhancement Ultimate Pleasure Recalled by Haute Health, LLC Due...

The Issue: Marketed without an Approved NDA/ANDA: Dietary supplement may contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 27, 2013· Haute Health, LLC

Recalled Item: Virilis Pro Recalled by Haute Health, LLC Due to Marketed without an...

The Issue: Marketed without an Approved NDA/ANDA: Dietary supplement may contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 27, 2013· Haute Health, LLC

Recalled Item: Prolifta Dietary Supplement Prolifta Recalled by Haute Health, LLC Due to...

The Issue: Marketed without an Approved NDA/ANDA: Dietary supplement may contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 26, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: LAMOTRIGINE TABLETS Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: CIPROFLOXACIN TABLETS Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 25, 2013· Sandoz Incorporated

Recalled Item: Hydroxychloroquine Sulfate Tablets Recalled by Sandoz Incorporated Due to...

The Issue: Failed Tablet/Capsule Specifications: Sandoz is recalling one lot of...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 24, 2013· W.S. Badger Company Inc.

Recalled Item: Badger Baby Broad Spectrum SPF 30 Zinc Oxide Sunscreen Lotion Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products; Selected lots of Badger...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2013· Hospira Inc.

Recalled Item: Metoclopramide Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Potential vendor glass issue - glass...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2013· Hospira Inc.

Recalled Item: Ondansetron Injection Recalled by Hospira Inc. Due to Presence of Particular...

The Issue: Presence of Particular Matter: Potential vendor glass issue - glass...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 24, 2013· W.S. Badger Company Inc.

Recalled Item: Badger Kids Broad Spectrum SPF30 Zinc Oxide Sunscreen Lotion Tangerine &...

The Issue: Microbial Contamination of Non-Sterile Products; Selected lots of Badger...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2013· Watson Laboratories Inc

Recalled Item: Next Choice" One Dose Emergency Contraceptive (Levonorgestrel Tablet)...

The Issue: Failed Tablet/Capsule Specifications: Multiple complaints for push through...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: Irinotecan Hydrochloride Injection Recalled by West-Ward Pharmaceutical...

The Issue: Superpotent Drug: a recent review of the USP revealed that an incorrect...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 23, 2013· Tolmar, Inc.

Recalled Item: Ketoconazole Shampoo Recalled by Tolmar, Inc. Due to Subpotent

The Issue: Subpotent

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

Class III — Low RiskOngoing
Refund
DrugSeptember 23, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: Irinotecan Hydrochloride Injection Recalled by West-Ward Pharmaceutical...

The Issue: Superpotent Drug: a recent review of the USP revealed that an incorrect...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 19, 2013· Ferring Pharmaceuticals Inc

Recalled Item: ENDOMETRIN (progesterone) Vaginal Insert 100 mg USP Recalled by Ferring...

The Issue: Discoloration; due to prolonged heat exposure.

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

Class III — Low RiskOngoing
Refund
DrugSeptember 17, 2013· Lupin Pharmaceuticals Inc.

Recalled Item: Quinapril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: During stability testing an...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 17, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Institutional, Inc. (d.b.a....

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund