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 1294112960 of 13,369 recalls

DrugOctober 8, 2012· GlaxoSmithKline, LLC.

Recalled Item: Arranon (nelarabine) Injection 5mg/mL Recalled by GlaxoSmithKline, LLC. Due...

The Issue: Impurities/Degradation Products: Potential for drug related impurities to...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2012· New England Compounding Center

Recalled Item: All Non Sterile Products manufactured by NECC (New England Compounding...

The Issue: GMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2012· New England Compounding Center

Recalled Item: All Sterile Products manufactured by NECC (New England Compounding Center)...

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
DrugOctober 5, 2012· Earthborn Products, Inc.

Recalled Item: Colloidal Silver Recalled by Earthborn Products, Inc. Due to Marketed...

The Issue: Marketed Without An Approved NDA/ANDA: This product is being recalled...

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

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

Recalled Item: Lactated Ringer's and 5% Dextrose Injection Recalled by Hospira Inc. Due to...

The Issue: Non-Sterility: One confirmed customer report that product contained...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 4, 2012· Hospira, Inc.

Recalled Item: Lidocaine HCl Injection Recalled by Hospira, Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Report of a vial containing visible...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 3, 2012· Paddock Laboratories, LLC

Recalled Item: Moexipril HCl Tablets 7.5mg Recalled by Paddock Laboratories, LLC Due to...

The Issue: Paddock Laboratories, LLC are recalling one lot (2012028142) of Moexipril...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 28, 2012· ITW Dymon

Recalled Item: Lemon Hand Sanitizing Wipes [n-alkyl dimethyl benzyl ammonium chloride...

The Issue: CGMP Deviations: The products were manufactured with raw material which...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2012· Genentech, Inc.

Recalled Item: CellCept (mycophenolate mofetil) capsules Recalled by Genentech, Inc. Due to...

The Issue: Short Fill: some bottles contained less than 120-count per labeled claim.

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2012· Dr. Reddy's Laboratories, Inc.

Recalled Item: Dr. Reddy's Quetiapine Fumarate Tablets Recalled by Dr. Reddy's...

The Issue: Failed USP Dissolution Test Requirements: During analysis of long term...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2012· Fresenius Kabi USA, LLC

Recalled Item: CYANOCOBALAMIN INJECTION Recalled by Fresenius Kabi USA, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility: Glass vials may have finish fractures and...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2012· Fresenius Kabi USA, LLC

Recalled Item: MIDAZOLAM HYDROCHLORIDE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Lack of Assurance of Sterility: Glass vials may have finish fractures and...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2012· Fresenius Kabi USA, LLC

Recalled Item: ONDANSETRON INJECTION Recalled by Fresenius Kabi USA, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility: Glass vials may have finish fractures and...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Methylprednisolone Acetate (PF) 40 mg/ml Injection Recalled by New England...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Glycerin 100% PF Recalled by New England Compounding Center 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
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Methylprednisolone Acetate 40 mg/mL Injection Recalled by New England...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Isovue 200 mg/mL PF and 300 mg/mL PF Recalled by New England Compounding...

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
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Omnipaque 240mg/mL PF Recalled by New England Compounding Center 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
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Saline 10% and 3% Recalled by New England Compounding Center 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
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Triamcinolone 10 mg/mL P Recalled by New England Compounding Center Due to...

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