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 87218740 of 13,369 recalls

DrugJune 27, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: Carvediol Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: Carvediol Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: Carvediol Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 27, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: buPROPion Hydrochloride Extended Release Tablets USP (SR) 150 mg Rx Recalled...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 24, 2016· Teva North America

Recalled Item: Amoxicillin for Oral Suspension USP Recalled by Teva North America Due to...

The Issue: Superpotent drug: Out of specification test result for assay during...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2016· Hospira Inc.

Recalled Item: Diazepam Injection USP 10mg/2mL (5 mg/mL Recalled by Hospira Inc. Due to...

The Issue: Crystallization: Product contains particulate identified to be crystallized...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 22, 2016· Teva North America

Recalled Item: Albuterol Sulfate Syrup Recalled by Teva North America Due to Presence of...

The Issue: Presence of Foreign Substance; presence of black particles describes...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 22, 2016· Mylan Pharmaceuticals Inc.

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

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: ARGATROBAN Injection in 0.9% Sodium Chloride 250 mg/250 mL (1 mg/mL)...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: Linezolid Injection 600 mg/300 mL Rx Only Recalled by Teva North America Due...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: Eptifibatide Injection 75 mg/100 mL (0.75 mg/mL) single use vial Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: Ondansetron Injection USP 40 mg/20 mL (2 mg/mL) Recalled by Teva North...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 13, 2016· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Methylprednisolone Tablets Recalled by Jubilant Cadista Pharmaceuticals,...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: incorrect expiration...

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

Class III — Low RiskOngoing
Refund
DrugJune 13, 2016· Sagent Pharmaceuticals Inc

Recalled Item: Oxacillin for Injection Recalled by Sagent Pharmaceuticals Inc Due to...

The Issue: Presence of Particulate Matter; The firm received two product complaints for...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 10, 2016· Valeant Pharmaceuticals North America LLC

Recalled Item: SECONAL SODIUM (secobarbital sodium) Capsules Recalled by Valeant...

The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...

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

Class III — Low RiskOngoing
Refund
DrugJune 3, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Sirolimus Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed impurities/degradation: out of specification result for impurity...

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

Class III — Low RiskOngoing
Refund
DrugJune 2, 2016· Exact-Rx Inc

Recalled Item: Urea (50% Urea in a Cream Base) Recalled by Exact-Rx Inc Due to...

The Issue: Crystallization; complaints received by the manufacturer of crystals forming...

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

Class III — Low RiskOngoing
Refund
DrugJune 1, 2016· Aidarex Pharmaceuticals LLC

Recalled Item: Ciprofloxacin OPTH 0.3% SOL Recalled by Aidarex Pharmaceuticals LLC Due to...

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

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

Class III — Low RiskOngoing
Refund
DrugJune 1, 2016· Aidarex Pharmaceuticals LLC

Recalled Item: CHLORHEXIDINE GLUCO. 0.12% ORAL RINSE Recalled by Aidarex Pharmaceuticals...

The Issue: Failed Impurity/Degradation Specifications: Out of specifications for...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2016· Teva North America

Recalled Item: mitoXANTRONE Injection USP (concentrate) Recalled by Teva North America Due...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class III — Low RiskOngoing
Refund