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. 2,270 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,270 in last 12 months

Showing 4794147960 of 48,326 recalls

Medical DeviceFebruary 9, 2012· Covidien LLC dba Uni-Patch

Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...

The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2012· Covidien LLC dba Uni-Patch

Recalled Item: Performa reusable and self-adhering TENS/NMES/FES stimulating electrodes...

The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2012· Covidien LLC dba Uni-Patch

Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...

The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2012· Afassco Inc

Recalled Item: The finger cots are made out of natural rubber. They Recalled by Afassco Inc...

The Issue: The firm is initiating a field correction because the product(s) were...

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

Class II — Potential Health HazardOngoing
DrugFebruary 6, 2012· sanofi-aventis US, Inc.

Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL Injection Recalled by...

The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2012· sanofi-aventis US, Inc.

Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL injection Recalled by...

The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 6, 2012· Metrex Research, LLC.

Recalled Item: CaviCide Recalled by Metrex Research, LLC. Due to Metrex Research is...

The Issue: Metrex Research is recalling Cavicide containing the Spring Fresh Fragrance...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2012· Accumetrics Inc

Recalled Item: VerifyNow P2Y12 Assay Recalled by Accumetrics Inc Due to The recall was...

The Issue: The recall was initiated by Accumetrics because of a field correction to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2012· Accumetrics Inc

Recalled Item: VerifyNow System Recalled by Accumetrics Inc Due to The recall was initiated...

The Issue: The recall was initiated by Accumetrics because of a field correction to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: *** 1) Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+3 Infusion Pump System Recalled by Hospira Inc. Due to Hospira has...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+ Hyperbaric Infusion Pump Recalled by Hospira Inc. Due to Hospira has...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2012· Orthosensor

Recalled Item: "****ORTHO SENSOR**12-123-A Knee Trial for Trithion***1560 Saw grass...

The Issue: Ortho sensor in Sunrise, FL is recalling the Graphics User Interface...

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

Class II — Potential Health HazardOngoing
DrugFebruary 3, 2012· Lloyd Inc

Recalled Item: Thyro-Tab 0.050mg. Recalled by Lloyd Inc Due to Subpotent (Single Ingredient...

The Issue: Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 3, 2012· Lloyd Inc

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc Due to...

The Issue: Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 1, 2012· Roche Molecular Systems, Inc.

Recalled Item: COBAS AmpliPrep Sample Tube Input Barcode Clips Recalled by Roche Molecular...

The Issue: Certain lots of COBAS AmpliPrep (CAP) S-tube Input (Box of 12 bags 12x24...

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

Class II — Potential Health HazardOngoing