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. 2,535 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,535 in last 12 months

Showing 91019120 of 13,369 recalls

DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Potassium Chloride Injection 20 mEq Recalled by Hospira Inc. Due to Chemical...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zoledronic Acid Injection Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Lack of Assurance of Sterility; defective seals where the metal silver ring...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 1, 2016· Sagent Pharmaceuticals Inc

Recalled Item: Fluconazole Injection Recalled by Sagent Pharmaceuticals Inc Due to Cross...

The Issue: Cross contamination with other products: metronidazole

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 29, 2016· Allegiant Health

Recalled Item: col-rite (docusate sodium) stool softener softgels Recalled by Allegiant...

The Issue: Superpotent Drug: High out of specification results for assay at the 6 month...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 25, 2016· Torrent Pharmaceuticals Limited

Recalled Item: Telmisartan Tablets Recalled by Torrent Pharmaceuticals Limited Due to...

The Issue: Presence of Foreign Substance: Product complaint for the presence of foreign...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 16, 2016· Genzyme Corporation

Recalled Item: Thyrogen (thyrotropin alfa for injection) Recalled by Genzyme Corporation...

The Issue: Presence of Particulate Matter: Glass particles found in the product after...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Genzyme Corporation

Recalled Item: Thyrogen (thyrotropin alfa for injection) Recalled by Genzyme Corporation...

The Issue: Presence of Particulate Matter: Glass particles found in the product after...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2016· Mylan Pharmaceuticals Inc.

Recalled Item: Paliperidone Extended-release Tablets Recalled by Mylan Pharmaceuticals Inc....

The Issue: Failed Dissolution Specifications; three month stability time point.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2016· Apace KY LLC

Recalled Item: Minocycline Hydrochloride Capsules USP Recalled by Apace KY LLC Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: the individual blisters...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 12, 2016· Ecolab Inc

Recalled Item: Scrub-Stat 4 (chlorhexidine gluconate) Foam Forming Solution Recalled by...

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
DrugFebruary 11, 2016· Sun Pharma Global Fze

Recalled Item: Alendronate Sodium Tablets Recalled by Sun Pharma Global Fze Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Observed levels of highest...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 11, 2016· J. Strickland and Co

Recalled Item: sulfur8 medicated LIGHT FORMULA (sulfur) anti-dandruff hair & scalp...

The Issue: Subpotent Drug: failed at the 3 and 6 month stability time points.

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

Class III — Low RiskOngoing
Refund
DrugFebruary 10, 2016· Pfizer Inc

Recalled Item: Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid Recalled by...

The Issue: Labeling: Label Mix-Up

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

Class III — Low RiskOngoing
Refund
DrugFebruary 9, 2016· Alcon Research, Ltd.

Recalled Item: TEARS Naturale FREE (dextran 70 and hypromellose 2910) lubricant eye drops...

The Issue: Lack of Assurance of Sterility: Some single-use vials may be filled with...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 8, 2016· Keystone Laboratories Inc

Recalled Item: Medicated Better Braids Recalled by Keystone Laboratories Inc Due to...

The Issue: Microbial Contamination of a Non-Sterile Products: The product had a...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2016· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Baxter Healthcare Corp. Due to...

The Issue: PRESENCE OF PARTICULATE MATTER: Product complaint for the presence of...

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

Class II — Potential Health HazardOngoing
Refund