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 1332113340 of 13,369 recalls

DrugApril 17, 2012· Watson Laboratories Inc

Recalled Item: Loxapine Capsules USP Recalled by Watson Laboratories Inc Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Package Insert: An outdated version of a...

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

Class III — Low RiskOngoing
Refund
DrugApril 17, 2012· Watson Laboratories Inc

Recalled Item: Loxitane Capsules Recalled by Watson Laboratories Inc Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Package Insert: An outdated version of a...

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

Class III — Low RiskOngoing
Refund
DrugApril 17, 2012· Watson Laboratories Inc

Recalled Item: Loxapine Capsules USP Recalled by Watson Laboratories Inc Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Package Insert: An outdated version of a...

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

Class III — Low RiskOngoing
Refund
DrugApril 16, 2012· Bracco Diagnostics Inc

Recalled Item: Bracco Diagnostics multihance (gadobenate dimeglumine) injection Recalled by...

The Issue: Short Fill: The product is being recalled due to a potential underfill of...

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

Class III — Low RiskOngoing
Refund
DrugApril 16, 2012· Bracco Diagnostics Inc

Recalled Item: Multihance Multipack (gadobenate dimeglumine) injection Recalled by Bracco...

The Issue: Lack of Assurance of Sterility; Product recalled due to displacement of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 11, 2012· Hospira, Inc.

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

The Issue: Presence of Particulate Matter: A single visible particulate was observed in...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 9, 2012· Dr. Reddy's Laboratories, Inc.

Recalled Item: Dr. Reddy's Amlodipine Besylate and Benazepril Hydrochloride 5 mg*/20 mg...

The Issue: Adulterated Presence of Foreign Tablets: Dr. Reddy's Laboratories has...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 9, 2012· Dr. Reddy's Laboratories, Inc.

Recalled Item: Dr. Reddy's Ciprofloxacin Tablets Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Adulterated Presence of Foreign Tablets: Dr. Reddy's Laboratories has...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2012· Hospira, Inc.

Recalled Item: Magnesium Sulfate in Water for Injection Recalled by Hospira, Inc. Due to...

The Issue: Superpotent (Single Ingredient) Drug: Above specification assay results for...

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

Class III — Low RiskOngoing
Refund
DrugApril 5, 2012· Apotex Corp.

Recalled Item: Meloxicam Tablets Recalled by Apotex Corp. Due to Tablet Thickness: Recall...

The Issue: Tablet Thickness: Recall was initiated due to the presence of one slightly...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 2, 2012· Teva Pharmaceuticals USA, Inc.

Recalled Item: Mefloquine HCL Tablets Recalled by Teva Pharmaceuticals USA, Inc. Due to...

The Issue: Tablet Thickness: Product is being recalled due to the potential of being...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 29, 2012· McKesson Packaging Services

Recalled Item: buPROPion Hydrochloride Extended-Release Tablets (XL) Recalled by McKesson...

The Issue: Failed USP Dissolution Test Requirements: Possible out-of-specification...

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

Class III — Low RiskOngoing
Refund
DrugMarch 29, 2012· McKesson Packaging Services

Recalled Item: buPROPion Hydrochloride Extended-Release Tablets (XL) Recalled by McKesson...

The Issue: Failed USP Dissolution Test Requirements: Possible out-of-specification...

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

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2012· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (Methylphenidate) Transdermal System Patch Recalled by Noven...

The Issue: Miscalibrated/Defective Delivery System; exceeded the specification for both...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 16, 2012· Ranbaxy Inc.

Recalled Item: Balnetar Therapeutic Tar Bath Recalled by Ranbaxy Inc. Due to Subpotent...

The Issue: Subpotent (Single Ingredient Drug): out-of-specification result for coal tar...

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

Class III — Low RiskOngoing
Refund
DrugMarch 14, 2012· Zydus Pharmaceuticals USA Inc

Recalled Item: Metformin Hydrochloride Tablets Recalled by Zydus Pharmaceuticals USA Inc...

The Issue: Presence of Foreign Substance(s): A product complaint was received from a...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2012· Pack Pharmaceuticals

Recalled Item: Ciprofloxacin Tablets Recalled by Pack Pharmaceuticals Due to Labeling...

The Issue: Labeling Illegible: Missing Label; The voluntary recall of the...

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

Class III — Low RiskOngoing
Refund
DrugMarch 9, 2012· Aurobindo Pharma LTD

Recalled Item: Northstar Zolpidem Tartrate Tablets USP 10 mg. Manufactured for Northstar RX...

The Issue: Adulterated Presence of Foreign Tablets: This product is being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2012· Lloyd Inc

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc Due to...

The Issue: Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2012· Lloyd Inc

Recalled Item: Thyro-Tab.075 mg. Recalled by Lloyd Inc Due to Subpotent (Single Ingredient...

The Issue: Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.

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

Class II — Potential Health HazardOngoing
Refund