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 30813100 of 27,852 recalls

Medical DeviceAugust 22, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: System Name: 722059 Allura Xper FD20/15 OR Table 722058 Allura Recalled by...

The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: System Name: 708038 MultiDiagnost Eleva with Flat Detector 708037...

The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2024· Intuitive Surgical, Inc.

Recalled Item: da Vinci 5 Recalled by Intuitive Surgical, Inc. Due to Surgical system Error...

The Issue: Surgical system Error 23062 due to connector1) Partially damaged "Potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2024· Olympus Corporation of the Americas

Recalled Item: Olympus Gastrointestinal Videoscope Recalled by Olympus Corporation of the...

The Issue: It was discovered during device performance testing that the CCD imaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2024· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: Horizon Cardiology Hemo. Version 12.2. Recalled by CHANGE HEALTHCARE CANADA...

The Issue: A potential issue has been identified in Change Healthcare Cardiology Hemo...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2024· XTANT Medical Holdings, Inc

Recalled Item: Cortera Spinal Fixation System Screw Recalled by XTANT Medical Holdings, Inc...

The Issue: Spinal fixation system implant screws marked "DNI" are not intended to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2024· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: Change Healthcare Cardiology Hemo. Versions 14.2 Recalled by CHANGE...

The Issue: A potential issue has been identified in Change Healthcare Cardiology Hemo...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2024· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: McKesson Cardiology Hemo. Versions 13.0 Recalled by CHANGE HEALTHCARE CANADA...

The Issue: A potential issue has been identified in Change Healthcare Cardiology Hemo...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur aTPO Assay Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Positive bias in patient results at and below the cut-off of 60 U/mL with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2024· Percussionaire Corporation

Recalled Item: Percussionaire Recalled by Percussionaire Corporation Due to Updated...

The Issue: Updated labeling to ensure that blue cap on in-line valve is removed, prior...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2024· Percussionaire Corporation

Recalled Item: Percussionaire Recalled by Percussionaire Corporation Due to Updated...

The Issue: Updated labeling to ensure that blue cap on in-line valve is removed, prior...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 21, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM aTPO Assay Recalled by Siemens Healthcare Diagnostics, Inc. Due...

The Issue: Positive bias in patient results at and below the cut-off of 60 U/mL with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2024· Ossur H / F

Recalled Item: Miami J Select Collar Recalled by Ossur H / F Due to Pressure sensitive...

The Issue: Pressure sensitive adhesive hooks attached to the sides of the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2024· Cypress Medical Products LLC

Recalled Item: BinaxNOW Respiratory Strep A Test Kit Recalled by Cypress Medical Products...

The Issue: Due to a classification error in our inventory management system, these...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2024· Cypress Medical Products LLC

Recalled Item: Acceava Respiratory Strep A Recalled by Cypress Medical Products LLC Due to...

The Issue: Due to a classification error in our inventory management system, these...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: basixTOUCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: Custom Inflation Kit Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: basixSKY Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: MONARCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: DiamondTOUCH Digital Inflation Device Recalled by Merit Medical Systems,...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing