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 1166111680 of 13,369 recalls

DrugDecember 23, 2013· Watson Laboratories Inc

Recalled Item: Carisoprodol Tablets Recalled by Watson Laboratories Inc Due to Presence of...

The Issue: Presence of Foreign Substance; metal particulates were visually observed in...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2013· Watson Laboratories, Inc.-(Actavis) - Florida

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by Watson...

The Issue: Failed Tablet/Capsule Specifications: Split tablets were found in the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2013· Carefusion 2200 Inc

Recalled Item: CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 15%...

The Issue: Subpotent Drug: CareFusion is recalling the CareFusion Scrub Care Surgical...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2013· Carefusion 2200 Inc

Recalled Item: CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 9%...

The Issue: Subpotent Drug: CareFusion is recalling the CareFusion Scrub Care Surgical...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 19, 2013· Abrams Royal Pharamacy

Recalled Item: All Unexpired Sterile Drug Products Recalled by Abrams Royal Pharamacy Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 19, 2013· Abrams Royal Pharamacy

Recalled Item: MINERAL IV Injection Recalled by Abrams Royal Pharamacy Due to...

The Issue: Non-Sterility; analytical results found product to contain Sphingomonas...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 18, 2013· Teva Pharmaceuticals USA

Recalled Item: Hydralazine HCL Tablets Recalled by Teva Pharmaceuticals USA Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:There is a potential for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 18, 2013· Teva Pharmaceuticals USA

Recalled Item: Hydralazine HCL Tablets Recalled by Teva Pharmaceuticals USA Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:There is a potential for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 16, 2013· Qualitest Pharmaceuticals

Recalled Item: Cetirizine Hydrochloride Syrup (Cetirizine Hydrochloride Oral Solution...

The Issue: Failed impurities/degradation specifications; out of specification for the...

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

Class III — Low RiskOngoing
Refund
DrugDecember 16, 2013· Bracco Diagnostics Inc

Recalled Item: VoLumen Barium Sulfate Suspension (0.1 % w/v Recalled by Bracco Diagnostics...

The Issue: Failed Stability Testing: This product is below specification for...

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

Class III — Low RiskOngoing
Refund
DrugDecember 13, 2013· Corepharma LLC

Recalled Item: Pyridostigmine Bromide Tablets USP Recalled by Corepharma LLC Due to Failed...

The Issue: Failed Dissolution Specification: Corepharma Inc. is recalling...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 12, 2013· Hospira Inc.

Recalled Item: Propofol Injectible Emulsion Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Glass defect located on the interior neck of...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 11, 2013· KVK-Tech, Inc.

Recalled Item: HydrOXYzine HCI Tablets USP 10 mg Recalled by KVK-Tech, Inc. Due to Good...

The Issue: Good Manufacturing Practices Deviations: The product has an Active...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 11, 2013· KVK-Tech, Inc.

Recalled Item: HydrOXYzine HCI Tablets USP 25 mg Recalled by KVK-Tech, Inc. Due to Good...

The Issue: Good Manufacturing Practices Deviations: The product has an Active...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 11, 2013· KVK-Tech, Inc.

Recalled Item: HydrOXYzine HCI Tablets USP 50 mg Recalled by KVK-Tech, Inc. Due to Good...

The Issue: Good Manufacturing Practices Deviations: The product has an Active...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 10, 2013· Slim Beauty USA

Recalled Item: Magic Slim capsules (Ling Zhi Recalled by Slim Beauty USA Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: The product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 10, 2013· Slim Beauty USA

Recalled Item: Dream Body Slimming Capsule (Chinese bitter orange 24% Recalled by Slim...

The Issue: Marketed Without An Approved NDA/ANDA: The product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 10, 2013· Slim Beauty USA

Recalled Item: Dr. Ming's Chinese Capsule (Ginger 50 mg Recalled by Slim Beauty USA Due to...

The Issue: Marketed Without An Approved NDA/ANDA: The product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 9, 2013· Actavis Inc

Recalled Item: Trelstar (triptorelin pamoate) for Injectable Suspension Single-Dose Vial...

The Issue: Labeling: Label Error On Declared Strength: Trelstar 11.25 mg labeled...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2013· Fresenius Kabi USA, LLC

Recalled Item: FOLIC ACID INJECTION Recalled by Fresenius Kabi USA, LLC Due to Failed...

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