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. 956 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
956 in last 12 months

Showing 31101–31120 of 47,938 recalls

Medical DeviceSeptember 28, 2016· Zimmer Biomet, Inc.

Recalled Item: Zimmer¿ Gender Solutions" Patellofemoral Joint Prosthesis Milling Handpiece...

The Issue: Complaints have been reported that the handpiece is inoperable. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS 4F Stiffened Micro-Introducer Recalled by Angiodynamics, Inc....

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
FoodSeptember 28, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Jalapeno Cherry Salsa. 21oz glass bottles and 1 Recalled by...

The Issue: Products contain yellow#5 ingredients not declared on the label.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 28, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Apple Riesling Salsa. 21oz glass bottles and 1 Recalled by...

The Issue: Products contain yellow#5 ingredients not declared on the label.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 28, 2016· Brownwood Farms

Recalled Item: Brownwood Farms BBQ Mustard Glaze. 11oz glass bottles and 1 Recalled by...

The Issue: Products contain soy ingredients not declared on the label.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 28, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Jalapeno Cherry Butter. 12oz glass bottles and 1 gallon....

The Issue: Products contain yellow#5 ingredients not declared on the label.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 28, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Peach Salsa. 17oz glass bottles. Private labels: Bowers...

The Issue: Products contain yellow#5 ingredients not declared on the label.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 28, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Cherry BBQ Sauce. 21oz glass bottles Recalled by Brownwood...

The Issue: Products contain soy ingredients not declared on the label.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 28, 2016· Brownwood Farms

Recalled Item: Brownwood Farms Yankee Bourbon BBQ Sauce. 19oz glass bottles and 1 gallon...

The Issue: Products contain soy ingredients not declared on the label.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 28, 2016· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Impurities/Degradation Specifications: out of specification result...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 28, 2016· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Clonazepam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Impurities/Degradation Specifications: out of specification result...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2016· Par Pharmaceutical, Inc.

Recalled Item: Gildess FE 1/20 (norethindrone acetate Recalled by Par Pharmaceutical, Inc....

The Issue: Subpotent Drug; Ethinyl Estradiol

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2016· Par Pharmaceutical, Inc.

Recalled Item: Gildess 1/20 (norethindrone acetate Recalled by Par Pharmaceutical, Inc. Due...

The Issue: Subpotent Drug; Ethinyl Estradiol

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2016· Par Pharmaceutical, Inc.

Recalled Item: Gildess 24 FE 1.5/30 (norethindrone acetate Recalled by Par Pharmaceutical,...

The Issue: Subpotent Drug; Ethinyl Estradiol

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: Mini Resupply Trauma Kit - Product Code 85-0835 Recalled by North American...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: Advance Trauma Kit - Product Code 85-0742 Recalled by North American Rescue...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: Range Trauma Kit Hardcase - Product Code 85-0889 Recalled by North American...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: Aid Backpack Kit - Product Code 85-0917 Recalled by North American Rescue...

The Issue: Lack of Assurance of Sterility: Concerns with product sterility by the...

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

Class II — Potential Health HazardOngoing
Refund