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. 2,322 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,322 in last 12 months

Showing 3828138300 of 48,326 recalls

FoodFebruary 20, 2015· White Wave Foods, Inc

Recalled Item: Organic Horizon Sandwich Crackers Cheddar Recalled by White Wave Foods, Inc...

The Issue: WhiteWave Foods is voluntarily recalling 7.5 oz packages of Horizon Cheddar...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 20, 2015· El Popocatepetl Ind., Inc.

Recalled Item: 8 in. sundried tomato flavored tortilla wraps Recalled by El Popocatepetl...

The Issue: El Popocatepetl Ind., Inc. of Chicago, Illinois is voluntarily recalling El...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 20, 2015· El Popocatepetl Ind., Inc.

Recalled Item: 8 in. chipotle flavored tortilla wraps Recalled by El Popocatepetl Ind.,...

The Issue: El Popocatepetl Ind., Inc. of Chicago, Illinois is voluntarily recalling El...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 20, 2015· El Popocatepetl Ind., Inc.

Recalled Item: 8 in. spinach pesto flavored tortilla wraps Recalled by El Popocatepetl...

The Issue: El Popocatepetl Ind., Inc. of Chicago, Illinois is voluntarily recalling El...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 20, 2015· Optimedica Corporation

Recalled Item: Catalys Precision Laser System-Catalys - U - US product Recalled by...

The Issue: Software anomaly on OptiMedica CATALYS System version 3.00.05 that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2015· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008 Series Hemodialysis Machines: 2008K with the following product code...

The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2015· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008 Series Hemodialysis Machines: 2008K2 with the following product code...

The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2015· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008 Series Hemodialysis Machines: 2008T with the following product code...

The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2015· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008 Series Hemodialysis Machines: 2008Kathome - 190895 2008T GEN 2 Recalled...

The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2015· Abbott Medical Optics, Inc.

Recalled Item: OptiMedica Catalys Precision Laser System Recalled by Abbott Medical Optics,...

The Issue: Device may experience loss of suction during treatment resulting in scoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2015· Pega Medical Inc.

Recalled Item: GAP Nail 4.8mm (diameter size) of the GAP ENDO-EXO MEDULLARY Recalled by...

The Issue: Failures of the 4.8mm of the GAP Endo-Exo Medullary System have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2015· ArthroCare Medical Corporation

Recalled Item: Coblator II System Recalled by ArthroCare Medical Corporation Due to The...

The Issue: The recalling firm was notified by the contract manufacturer that they had...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2015· Steris Corporation

Recalled Item: Caviwave Pro Ultrasonic Cleaning System Recalled by Steris Corporation Due...

The Issue: Should the Caviwave Pro Ultrasonic Cleaning System experience a temporary...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2015· Steris Corporation

Recalled Item: AMSCO C and AMSCO 400 Steam Sterilizers Recalled by Steris Corporation Due...

The Issue: STERIS has identified that the control board software in select AMSCO 400...

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

Class II — Potential Health HazardOngoing
DrugFebruary 18, 2015· Mylan Institutional LLC

Recalled Item: Haloperidol Decanoate Injection Recalled by Mylan Institutional LLC Due to...

The Issue: Lack of Assurance of Sterility; due to leaking vials

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 18, 2015· Mylan Institutional LLC

Recalled Item: Haloperidol Decanoate Injection Recalled by Mylan Institutional LLC Due to...

The Issue: Lack of Assurance of Sterility; due to leaking vials

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 18, 2015· CHG Hospital Beds Inc

Recalled Item: The Spirit TM Select bed is a Med-Surg bed intended Recalled by CHG Hospital...

The Issue: It was identified that in some situations the bed exit alarm may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2015· US Endoscopy Group Inc

Recalled Item: Velocity" Biopsy Valve Recalled by US Endoscopy Group Inc Due to The company...

The Issue: The company has received reports of structural non conformance at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2015· King Systems Corp.

Recalled Item: Double Swivel Connector with Suction Port Connector Recalled by King Systems...

The Issue: Product is mislabeled as Double Swivel Connector with Suction Port and is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2015· Transonic Systems Inc

Recalled Item: Transonic Hemodialysis Monitor Recalled by Transonic Systems Inc Due to...

The Issue: Customer unable to obtain measurements due to the device seeing no flow or...

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

Class II — Potential Health HazardOngoing