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 2570125720 of 48,326 recalls

DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: LIPO-PLEX Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr....

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: PYRIDOXINE Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr....

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: ADENO-PLEX Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr....

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: LIPO-DEN EXTREME Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr....

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: METHYLCOBALAMIN Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr....

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: LIPO-DEN Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr....

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: LIPO-DEN PLUS Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr....

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: HYDROXOCOBALAMIN Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park...

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2018· Coastal Meds, LLC.

Recalled Item: CYANOCOBALAMIN Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr....

The Issue: Presence of Particulate matter. Recall due to presence of unknown...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 4, 2018· Handpiece Headquarters

Recalled Item: Henry Schein CU 1000 Halogen Curing Light Recalled by Handpiece Headquarters...

The Issue: Tip of the curing light was too hot causing a heat sensation in the patients.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2018· Deerfield Imaging, Inc.

Recalled Item: IMRIS IMRI 1.5T AND 3T S System Product Usage: The Recalled by Deerfield...

The Issue: The DC power to the IFOSS collision detector control panel at your facility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2018· Menarini Silicon Biosystems

Recalled Item: CELLSEARCH¿ CIRCULATING Tumor Cell Kits (IVD) (Product Code 7900001)...

The Issue: Unusually high number of total images/unassigned events may require...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...

The Issue: Service technician improperly documented final release testing on product,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...

The Issue: Service technician improperly documented final release testing on product,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...

The Issue: Service technician improperly documented final release testing on product,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...

The Issue: Service technician improperly documented final release testing on product,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...

The Issue: Service technician improperly documented final release testing on product,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Modular Head Component Recalled by Zimmer Biomet, Inc. Due to Two lots of...

The Issue: Two lots of different sized modular heads potentially commingled. Risks...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2018· Synthes (USA) Products LLC

Recalled Item: Retractor f/Sciatic Nerve Long Recalled by Synthes (USA) Products LLC Due to...

The Issue: There is a potential for microspores to form on the hollow handle of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 2, 2018· Synthes (USA) Products LLC

Recalled Item: Retractor f/Sciatic Nerve Recalled by Synthes (USA) Products LLC Due to...

The Issue: There is a potential for microspores to form on the hollow handle of the...

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

Class II — Potential Health HazardOngoing