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. 2,371 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,371 in last 12 months

Showing 2680126820 of 48,326 recalls

FoodNovember 1, 2017· doTERRA International, LLC

Recalled Item: Slim & Sassy¿ TrimShake Vanilla Recalled by doTERRA International, LLC Due...

The Issue: doTERRA is voluntarily recalling unexpired Slim & Sassy¿ TrimShake -...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 1, 2017· Aurora Products, Inc.

Recalled Item: Aurora Brand Dark Chocolate Cherries packaged in: 8.5 oz. Plastic Recalled...

The Issue: Product contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2017· Aurora Products, Inc.

Recalled Item: Dark Chocolate Cranberries packaged in: Bulk 3.5 oz. Plastic Cup Recalled by...

The Issue: Product contains undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2017· doTERRA International, LLC

Recalled Item: Slim & Sassy¿ TrimShake Chocolate Recalled by doTERRA International, LLC Due...

The Issue: doTERRA is voluntarily recalling unexpired Slim & Sassy¿ TrimShake -...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 1, 2017· Ion Beam Applications S.A.

Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to The internal...

The Issue: The internal configuration of the electrometers and the Real-Time control...

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

Class II — Potential Health HazardOngoing
FoodOctober 31, 2017· Shoreline Fruit, LLC

Recalled Item: Shoreline Fruit Dark Choc Covered Montmorency Cherries packaged in 25-pound...

The Issue: Shoreline Fruit is voluntarily recalling select Shoreline Fruit bulk and...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 31, 2017· Shoreline Fruit, LLC

Recalled Item: Dried Dark Chocolate Covered Cherries Recalled by Shoreline Fruit, LLC Due...

The Issue: Shoreline Fruit is voluntarily recalling select Shoreline Fruit bulk and...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 30, 2017· Pharmedium Services, LLC

Recalled Item: ePHEDrine Sulfate In 0.9% Sodium Chloride Recalled by Pharmedium Services,...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 30, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol Recalled by Dr....

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date; lot number on the...

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

Class III — Low RiskOngoing
Refund
DrugOctober 30, 2017· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Meclizine hydrochloride tablets USP Recalled by Jubilant Cadista...

The Issue: Marketed without an approved NDA/ANDA: Bottles were released prior to final...

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

Class III — Low RiskOngoing
Refund
FoodOctober 30, 2017· 21ST CENTURY SNACK FOODS

Recalled Item: 21st CENTURY SNACK FOODS DARK CHOCOLATE ALMONDS Roasted Almonds Covered...

The Issue: Product contains undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 30, 2017· ICU Medical Inc

Recalled Item: ICU Mednet(TM) Medication Management Suite 6.1 and 6.21 Recalled by ICU...

The Issue: Issue 1: The MedNet Meds 6.1 and 6.21 programs, under certain conditions,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2017· ICU Medical Inc

Recalled Item: Plum 360 Infusion System Recalled by ICU Medical Inc Due to (1) Under...

The Issue: (1) Under certain conditions, if a malfunction alarm occurs while the pump...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2017· NordicNeuroLab AS

Recalled Item: fMRI Hardware System - AudioSystem Recalled by NordicNeuroLab AS Due to...

The Issue: Report was of an interrupted MR scan after patient complained about acoustic...

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

Class II — Potential Health HazardOngoing
DrugOctober 27, 2017· Fresenius Kabi USA, LLC

Recalled Item: Midazolam Injection Recalled by Fresenius Kabi USA, LLC Due to Labeling:...

The Issue: Labeling: Label MIX-UP. Blister Packages, Labeled as Midazolam injection,...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 27, 2017· L3 Security & Detection

Recalled Item: L3 Security & Detection System Cabinet X-ray system used for Recalled by L3...

The Issue: L3 has determined in airport environments, there have been several cases...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2017· Physio-Control, Inc.

Recalled Item: LIFEPAK(R) Electrode Starter Kits Recalled by Physio-Control, Inc. Due to...

The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 27, 2017· Physio-Control, Inc.

Recalled Item: LIFEPAK(R) defibrillation electrodes Recalled by Physio-Control, Inc. Due to...

The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing