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. 2,349 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,349 in last 12 months

Showing 3376133780 of 48,326 recalls

FoodFebruary 11, 2016· International Foodsource, LLC

Recalled Item: IFS Club Bag Pistachio Raw Shelled 80% Wholes Net Wt. Recalled by...

The Issue: Raw pistachios may be contaminated with Salmonella which was determined...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 11, 2016· International Foodsource, LLC

Recalled Item: Sam International Bulk Raw Whole Pistachio 80% VP Net Wt. Recalled by...

The Issue: Raw pistachios may be contaminated with Salmonella which was determined...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 11, 2016· International Foodsource, LLC

Recalled Item: IFS Web Bulk Pistachio Raw Shelled 80% Wholes Net Wt. Recalled by...

The Issue: Raw pistachios may be contaminated with Salmonella which was determined...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 11, 2016· Health Matters America, Inc.

Recalled Item: Organic traditions SPROUTED CHIA & FLAX SEED POWDER Recalled by Health...

The Issue: The repacked product has the potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 11, 2016· Health Matters America, Inc.

Recalled Item: Organic traditions SPROUTED FLAX SEED POWDER Recalled by Health Matters...

The Issue: The repacked product has the potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 11, 2016· Cary's of Oregon LLC

Recalled Item: Carys Dark Chocolate Almond Toffee with Hawaiian Salt. Product is Recalled...

The Issue: Carys Dark Chocolate Almond Toffee with Hawaiian Salt is recalled because...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 11, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: Accu-Chek Inform II Base Unit as a part of the Recalled by Roche Diagnostics...

The Issue: Accu-Chek Inform II Base Unit might produce physical transmission errors in...

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

Class II — Potential Health HazardOngoing
DrugFebruary 10, 2016· Pfizer Inc

Recalled Item: Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid Recalled by...

The Issue: Labeling: Label Mix-Up

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 10, 2016· Philips Electronics North America Corporation

Recalled Item: evaluemed Infant Heel Warmer 301-1223 Recalled by Philips Electronics North...

The Issue: eValueMed Infant Heel Warmers and eValueMed Infant Transport Mattresses bear...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2016· Philips Electronics North America Corporation

Recalled Item: eValueMed Infant Transport Mattress 301-1015 Recalled by Philips Electronics...

The Issue: eValueMed Infant Heel Warmers and eValueMed Infant Transport Mattresses bear...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2016· Focus Diagnostics Inc

Recalled Item: Simplexa Group A Strep Direct (MOL2850) with Direct Amplification Disc...

The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Focus Diagnostics Inc

Recalled Item: Simplexa HSV 1&2 Direct (MOL2150) with Direct Amplification Disc (MOL1451...

The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Focus Diagnostics Inc

Recalled Item: Simplexa Flu A/B & RSV Direct (MOL2650) with Direct Amplification Disc...

The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Percutaneous Insertion Tray Recalled by Arrow International, Inc., Division...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Ultra 8 IAB: 8Fr 40cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: Ultra 8 IAB: 8Fr 30cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: RediGuard IAB: 7Fr 30cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: UltraFlex IAB: 7.5Fr 30cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: FiberOptix Ultra 8 IAB: 8Fr 30cc The Arrow¿ IAB is Recalled by Arrow...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2016· Arrow International, Inc., Division of Teleflex Medical Inc.

Recalled Item: UltraFlex IAB: 7.5Fr 40cc Recalled by Arrow International, Inc., Division of...

The Issue: The sheath body may become separated from the sheath hub. If the separation...

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

Class I — Serious Health HazardOngoing