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 1152111540 of 13,369 recalls

DrugMarch 20, 2014· Apotex Inc.

Recalled Item: Risperidone Oral Solution Recalled by Apotex Inc. Due to Failed...

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

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

Class III — Low RiskOngoing
Refund
DrugMarch 20, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Venlafaxine Hydrochloride Extended-Release Tablets Recalled by Caraco...

The Issue: Failed Dissolution Specifications: Stability results found the product did...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 18, 2014· Glenmark Generics Inc., USA

Recalled Item: Ranitidine Tablets USP Recalled by Glenmark Generics Inc., USA Due to...

The Issue: Presence of Foreign Tablets/Capsules: Recall is due to a pharmacist...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2014· Shire Human Genetic Therapies, Inc.

Recalled Item: VPRIV¿ (velaglucerase alfa for injection) Recalled by Shire Human Genetic...

The Issue: Presence of Particulate Matter; Particulates identified as stainless steel...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 13, 2014· Pain Free By Nature

Recalled Item: REUMOFAN PLUS Tablets Recalled by Pain Free By Nature Due to Undeclared...

The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 11, 2014· Paddock Laboratories, LLC

Recalled Item: Perrigo Recalled by Paddock Laboratories, LLC Due to Presence of Particulate...

The Issue: Presence of Particulate Matter Perrigo is recalling seven lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2014· AbbVie Inc

Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2014· AbbVie Inc

Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2014· AbbVie Inc

Recalled Item: LUPRON DEPOT-PED (Leuprolide Acetate for Depot Suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2014· AbbVie Inc

Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may containin a syringe...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2014· AbbVie Inc

Recalled Item: Lupron Depot (leuprolide acetate for depot suspension) Single Dose...

The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 6, 2014· Pfizer Us Pharmaceutical Group

Recalled Item: Effexor XR (venlafaxine HCl) Extended-Release Capsules Recalled by Pfizer Us...

The Issue: Presence of Foreign Tablets/Capsules: A Pharmacist reported that a bottle of...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 6, 2014· Greenstone Llc

Recalled Item: Venlafaxine HCl Extended-Release Capsules Recalled by Greenstone Llc Due to...

The Issue: Presence of Foreign Tablets/Capsules: report of a foreign capsule with...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 4, 2014· Alkermes, Inc.

Recalled Item: VIVITROL (naltrexone for extended-release injectable suspension) Recalled by...

The Issue: Customer complaints for failure to deliver the dose.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2014· Teva Pharmaceuticals USA

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Teva Pharmaceuticals USA Due...

The Issue: Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2014· Teva Pharmaceuticals USA

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Teva Pharmaceuticals USA Due...

The Issue: Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2014· Teva Pharmaceuticals USA

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Teva Pharmaceuticals USA Due...

The Issue: Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2014· Sagent Pharmaceuticals Inc

Recalled Item: Zoledronic Acid Injection 5 mg per 100 mL (0.05 mg/mL) Recalled by Sagent...

The Issue: Lack of Assurance of Sterility; leaking of premix bags

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not PORTABLE SIPS Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 3, 2014· Terra-Medica Inc.

Recalled Item: Pleo Not OINTMENT 3X Recalled by Terra-Medica Inc. Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund