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 1292112940 of 13,369 recalls

DrugOctober 24, 2012· GlaxoSmithKline, LLC.

Recalled Item: Advair HFA (fluticasone propionate/salmeterol) Inhalation Aerosol Recalled...

The Issue: Product Lacks Stability: These lots are being recalled due to the failure to...

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

Class III — Low RiskOngoing
Refund
DrugOctober 23, 2012· Estee Lauder Inc

Recalled Item: ESTEE LAUDER DayWear Sheer Tint Release Recalled by Estee Lauder Inc Due to...

The Issue: Failed Stability Specifications: The active sunscreen ingredient, avobenzone...

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

Class III — Low RiskOngoing
Refund
DrugOctober 22, 2012· Hospira Inc.

Recalled Item: HEXTEND 6% Hetastarch in Lactated Electrolyte Injection Recalled by Hospira...

The Issue: Lack of Assurance of Sterility: There is the potential for the solution to...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2012· Zi Xiu Tang Success, LLC

Recalled Item: Ultimate Formula Recalled by Zi Xiu Tang Success, LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Products were found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 22, 2012· Zi Xiu Tang Success, LLC

Recalled Item: Classic Zi Xiu Tang Recalled by Zi Xiu Tang Success, LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Products were found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 19, 2012· Watson Laboratories Inc

Recalled Item: Zovia (ethynodiol diacetate and ethinyl estradiol) Tablets USP Recalled by...

The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2012· Watson Laboratories Inc

Recalled Item: Zenchent (norethindrone and ethinyl estradiol) Tablets USP Recalled by...

The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2012· Watson Laboratories Inc

Recalled Item: Necon 1/35-28 (norethindrone and ethinyl estradiol) Tablets USP Recalled by...

The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2012· Watson Laboratories Inc

Recalled Item: Lutera (levonorgestrel and ethinyl estradiol) Tablets USP Recalled by Watson...

The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2012· Watson Laboratories Inc

Recalled Item: Necon 10/11 (norethindrone and ethinyl estradiol) Tablets USP Recalled by...

The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree Oil-Free Acne Cleanser (benzoyl peroxide 2.5% w/v) Recalled by...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

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

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree 24 Hour Severe Acne Clearing System containing 1-count 4 Recalled...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

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

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree Acne Pore Cleanser (benzoyl peroxide 2.5% w/v) Recalled by Valeant...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

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

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree 3-in-1 Acne Night Repair Foam (retinol + salicylic acid 1.5% w/v)...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

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

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree Acne Astringent Toner Pads (salicylic acid 2% w/v) Recalled by...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

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

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree Severe Maximum Strength Acne Pore Cleanser (benzoyl peroxide 5%...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

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

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree Original Strength Terminator (benzoyl peroxide 5% w/v) Recalled by...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

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

Class III — Low RiskOngoing
Refund
DrugOctober 15, 2012· Valeant Pharmaceuticals

Recalled Item: AcneFree 24 Hour Clearing System containing 1-count 4 fl oz Recalled by...

The Issue: Subpotent (Single Ingredient) Drug: This product was found to be subpotent...

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

Class III — Low RiskOngoing
Refund
DrugOctober 11, 2012· Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Recalled Item: Perphenazine Tablets Recalled by Vintage Pharmaceuticals LLC DBA Qualitest...

The Issue: Tablet Separation: Possibility of cracked or split coating on the tablets.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2012· American Health Packaging

Recalled Item: QUETIAPINE Fumarate Tablets 25mg 100 Tablets (10x10) Blister card Recalled...

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

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

Class II — Potential Health HazardOngoing
Refund