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 87418760 of 13,369 recalls

DrugMay 30, 2016· Prinston Pharmaceutical Inc

Recalled Item: Irbesartan and Hydrochlorothiazide Tablets Recalled by Prinston...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Incorrect lot number,...

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

Class III — Low RiskOngoing
Refund
DrugMay 28, 2016· Par Pharmaceutical

Recalled Item: Pramipexole Dihydrochloride Extended Release Tablets Recalled by Par...

The Issue: Failed Impurities/Degradation Specifications: Par Pharmaceutical is...

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

Class III — Low RiskOngoing
Refund
DrugMay 26, 2016· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Kamedis BIO-HERBAL DANDRUFF CARE THERAPEUTIC 2-STEP DANDRUFF CARE SYSTEM -...

The Issue: Subpotent Drug: Out of Specification assay values on stability for the...

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

Class III — Low RiskOngoing
Refund
DrugMay 26, 2016· Stratus Pharmaceuticals Inc

Recalled Item: Remeven Cream Recalled by Stratus Pharmaceuticals Inc Due to...

The Issue: Crystallization; Complaints that cream appears to have crystallized

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

Class III — Low RiskOngoing
Refund
DrugMay 25, 2016· Sandoz Inc

Recalled Item: Lisinopril Tablets USP Recalled by Sandoz Inc Due to Labeling: Incorrect or...

The Issue: Labeling: Incorrect or Missing Package Insert

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

Class III — Low RiskOngoing
Refund
DrugMay 23, 2016· Nostrum Laboratories, Inc.

Recalled Item: Nitrofurantoin Oral Suspension Recalled by Nostrum Laboratories, Inc. Due to...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 23, 2016· Valeant Pharmaceuticals North America LLC

Recalled Item: Lodrane D (Brompheniramine maleate 4 mg and Pseudoephedrine HCl 60 mg)...

The Issue: Labeling: Not Elsewhere Classified: correctly labeled bottles were packaged...

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

Class III — Low RiskOngoing
Refund
DrugMay 19, 2016· West-Ward Columbus Inc

Recalled Item: Oxycodone HCl Recalled by West-Ward Columbus Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specification; 9 month stability

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

Class III — Low RiskOngoing
Refund
DrugMay 19, 2016· Galderma Laboratories, L.P.

Recalled Item: Doxycycline Recalled by Galderma Laboratories, L.P. Due to Labeling:...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: Some expiries and lot...

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

Class III — Low RiskOngoing
Refund
DrugMay 18, 2016· Teva North America

Recalled Item: Divalproex Sodium Delayed-release Tablets USP Recalled by Teva North America...

The Issue: Failed Tablet/Capsule Specifications

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Akorn, Inc.

Recalled Item: Sulfacetamide Sodium Ophthalmic Solution Recalled by Akorn, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility; some lots failed Antimicrobial Effectiveness...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 17, 2016· Clinique International

Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...

The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...

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

Class III — Low RiskOngoing
Refund
DrugMay 16, 2016· Virtus Pharmaceuticals, Llc

Recalled Item: VP-CH-PNV Prenatal/Postnatal capsules Recalled by Virtus Pharmaceuticals,...

The Issue: Defective delivery system: Softgel capsules are leaking.

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

Class III — Low RiskOngoing
Refund
DrugMay 13, 2016· Medaus, Inc.

Recalled Item: B-COMPLEX 50 IN NACL 0.9% W/PRES. Recalled by Medaus, Inc. Due to Lack of...

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
DrugMay 13, 2016· Medaus, Inc.

Recalled Item: MINOXIDIL 0.5% W/PRES. (BENZYL ETOH 2%) Recalled by Medaus, Inc. Due to Lack...

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