Product Recalls in Montana

Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,359 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,359 in last 12 months

Showing 3110131120 of 48,326 recalls

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
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 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
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· North American Rescue LLC.

Recalled Item: USCG Boat Response Kit - Product Code 80-0353 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· 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 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· Par Pharmaceutical, Inc.

Recalled Item: Gildess 1.5/30 (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 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· 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· 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
DrugSeptember 27, 2016· North American Rescue LLC.

Recalled Item: Amphibious Trauma Kit - Product Code 85-0639 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: Range Trauma Kit - Product Code 85-1274 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: K-9 Trauma Field Kit - Product Code 80-0211 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: 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: Range Trauma Kit ORG - Product Code 80-0213 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
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: ART/CVP KIT W/03ML FLUSH DEVICE FOR MILWAUKEE CHILDRENS HOSP. Recalled by...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing