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. 2,334 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,334 in last 12 months

Showing 3754137560 of 48,326 recalls

FoodApril 15, 2015· Reaction Nutrition LLC

Recalled Item: Bio Armor Carno Pump Plus Electrolytes 40 servings (Cherry Lime) Recalled by...

The Issue: Work out support nutritional supplements manufactured on shared equipment...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 15, 2015· Reaction Nutrition LLC

Recalled Item: REACTION RECOR: Amino Action- 500g (Island Breeze) Recalled by Reaction...

The Issue: Work out support nutritional supplements manufactured on shared equipment...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 15, 2015· Reaction Nutrition LLC

Recalled Item: Bio Armor CreaMatrix 60 servings Cherry Lime Recalled by Reaction Nutrition...

The Issue: Work out support nutritional supplements manufactured on shared equipment...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 15, 2015· Reaction Nutrition LLC

Recalled Item: Bio Armor CreaMatrix 60 servings Blue Raspberry Recalled by Reaction...

The Issue: Work out support nutritional supplements manufactured on shared equipment...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity Core 128 Computed Tomography X-ray system...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity Core Computed Tomography X-ray system Recalled...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Ingenuity CT Computed Tomography X-ray system Recalled by...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare Brilliance 64 Computed Tomography X-ray system Recalled...

The Issue: During scans with specific protocol steps, the software unexpectedly sets...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM ARISTOS FX Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the cable cart and the corrugated hose are unable to move freely, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2015· Halyard Health, Inc

Recalled Item: KimVent Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...

The Issue: The internal blue flapper valve of certain KimVent Turbo-Cleaning Closed...

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

Class II — Potential Health HazardOngoing
DrugApril 14, 2015· Actavis Laboratories

Recalled Item: Flurandrenolide Tape Recalled by Actavis Laboratories Due to Subpotent Drug:...

The Issue: Subpotent Drug: Flurandrenolide is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: EPINEPHrine HCl 1 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: HEPARIN Sodium Injection USP Recalled by Pharmedium Services, LLC Due to...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: EPINEPHrine HCl 4 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: EPINEPHrine HCl 16 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2015· Teva Pharmaceuticals USA

Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...

The Issue: Chemical Contamination: Product recalled due to an elevated level of a...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2015· Teva Pharmaceuticals USA

Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...

The Issue: Chemical Contamination: Product recalled due to an elevated level of a...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2015· Hospira Inc.

Recalled Item: Ketorolac Tromethamine Inj. USP Recalled by Hospira Inc. Due to Crystallization

The Issue: Crystallization

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2015· Hospira Inc.

Recalled Item: Ketorolac Tromethamine Inj. USP Recalled by Hospira Inc. Due to Crystallization

The Issue: Crystallization

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2015· Pharmedium Services, LLC

Recalled Item: HEPARIN Sodium Injection USP 25 Recalled by Pharmedium Services, LLC Due to...

The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...

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

Class I — Serious Health HazardOngoing
Refund