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. 2,568 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,568 in last 12 months

Showing 25012520 of 27,852 recalls

Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) VP SHUNT CDS Recalled...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· Medtronic Neuromodulation

Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable Recalled...

The Issue: Software issues were identified in application version 2.x.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) MEM MAXILLOFACIAL...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) MICRODISECTOMY PACK...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) NASAL PACK Recalled by...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) ENDOSCOPIC SKULL BASE...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) FREE FLAP Recalled by...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) CRANI Recalled by...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: See DocMan Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Custom...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· Medtronic Neuromodulation

Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable Recalled...

The Issue: Software issues were identified in application version 2.x.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: See DocMan Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Custom...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) UMC DR. BAKER...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· Medtronic Neuromodulation

Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable Recalled...

The Issue: Software issues were identified in application version 2.x.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline custom medical procedure kits labeled as: 1) PANENDOSCOPY-LF...

The Issue: Custom convenience kits are being recall because the contain non-sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· Abbott Medical

Recalled Item: The Merlin PCS 3650 programmer Model 3330 The Merlin PCS Recalled by Abbott...

The Issue: Due to a programmer software anomaly, during finalizing of the leadless...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· GE OEC Medical Systems, Inc

Recalled Item: OEC 3D Fluoroscopic X-Ray System Recalled by GE OEC Medical Systems, Inc Due...

The Issue: Due to manufacturing issue of insufficient sealing of X-ray tubes and can...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· GE OEC Medical Systems, Inc

Recalled Item: OEC Elite Fluoroscopic X-Ray System Recalled by GE OEC Medical Systems, Inc...

The Issue: Due to manufacturing issue of insufficient sealing of X-ray tubes and can...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· GE OEC Medical Systems, Inc

Recalled Item: OEC 9900 Fluoroscopic X-Ray System Recalled by GE OEC Medical Systems, Inc...

The Issue: Due to manufacturing issue of insufficient sealing of X-ray tubes and can...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2024· GE OEC Medical Systems, Inc

Recalled Item: OEC 9800 Fluoroscopic X-Ray System Recalled by GE OEC Medical Systems, Inc...

The Issue: Due to manufacturing issue of insufficient sealing of X-ray tubes and can...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2024· Nova Biomedical Corporation

Recalled Item: StatStrip Glucose Hospital Meter System. Model/Catalog Number: 63685....

The Issue: A software bug within the Gen 2 StatStrip Hospital Meter firmware leads to...

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

Class I — Serious Health HazardOngoing