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. 1,876 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
1,876 in last 12 months

Showing 1562115640 of 27,852 recalls

Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· ESAOTE S.P.A.

Recalled Item: MyLab Seven Recalled by ESAOTE S.P.A. Due to The probe power monitoring...

The Issue: The probe power monitoring settings have been found to be not appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· ESAOTE S.P.A.

Recalled Item: MyLab Alpha Recalled by ESAOTE S.P.A. Due to The probe power monitoring...

The Issue: The probe power monitoring settings have been found to be not appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Cardinal Health 200, LLC

Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...

The Issue: The suction valve may not close properly which could cause continuous suction.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· ESAOTE S.P.A.

Recalled Item: MyLab Gamma Recalled by ESAOTE S.P.A. Due to The probe power monitoring...

The Issue: The probe power monitoring settings have been found to be not appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2018· Withings Sas

Recalled Item: Nokia BPM+ Wireless Blood Pressure Monitor Product System Recalled by...

The Issue: Device could not meet the requirements for systolic pressure

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Bio-Rad Laboratories, Inc

Recalled Item: MRSASelect Recalled by Bio-Rad Laboratories, Inc Due to Abnormal coloration...

The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Bio-Rad Laboratories, Inc

Recalled Item: MRSASelect II Recalled by Bio-Rad Laboratories, Inc Due to Abnormal...

The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing