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. 2,530 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,530 in last 12 months

Showing 89819000 of 27,852 recalls

Medical DeviceAugust 16, 2021· Olympus Corporation of the Americas

Recalled Item: BF-XT160 EVIS EXERA Bronchovideoscope Recalled by Olympus Corporation of the...

The Issue: The firm is issuing validated, new reprocessing instructions according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Biodex Medical Systems, Inc.

Recalled Item: AtomLab 500Plus Dose CalibratorSoftware 2.0.00 through Revision 2.0.08...

The Issue: When deleting a previously entered custom isotope, the software deletes the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Olympus Corporation of the Americas

Recalled Item: BF-1T60 OES Bronchofiberscope Recalled by Olympus Corporation of the...

The Issue: The firm is issuing validated, new reprocessing instructions according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Olympus Corporation of the Americas

Recalled Item: BF-N20 OES Bronchofiberscope Recalled by Olympus Corporation of the Americas...

The Issue: The firm is issuing validated, new reprocessing instructions according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Olympus Corporation of the Americas

Recalled Item: BF-P60 OES Bronchofiberscope Recalled by Olympus Corporation of the Americas...

The Issue: The firm is issuing validated, new reprocessing instructions according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Olympus Corporation of the Americas

Recalled Item: BF-Q180-AC EVIS EXERA II Bronchovideoscope Recalled by Olympus Corporation...

The Issue: The firm is issuing validated, new reprocessing instructions according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Olympus Corporation of the Americas

Recalled Item: BF-XP160F EVIS EXERA Bronchovideoscope Recalled by Olympus Corporation of...

The Issue: The firm is issuing validated, new reprocessing instructions according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Olympus Corporation of the Americas

Recalled Item: BF-P180 EVIS EXERA II Bronchovideoscope Recalled by Olympus Corporation of...

The Issue: The firm is issuing validated, new reprocessing instructions according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.CT VA20A Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for data loss when using the contouring or patient marking...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via RT Image Suite with syngo.via VB30 Recalled by Siemens Medical...

The Issue: Potential for data loss when using the contouring or patient marking...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: MR MAGNETOM Systems with RT Image Suite with syngo MR VA20A Recalled by...

The Issue: Potential for data loss when using the contouring or patient marking...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2021· IMPERATIVE CARE INC

Recalled Item: Imperative Care Recalled by IMPERATIVE CARE INC Due to There is a potential...

The Issue: There is a potential for distal end of catheters to fracture and become...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 13, 2021· Philips North America Llc

Recalled Item: The Allura Xper series is intended for use on human Recalled by Philips...

The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2021· Philips North America Llc

Recalled Item: The Azurion series (within the limits of the used Operation Recalled by...

The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2021· Quidel Corporation

Recalled Item: Lyra Direct SARS-CoV-2 Assay Emergency Use Authorization- . The Recalled by...

The Issue: Revised Instructions for Use: Potential for specimens from patients with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2021· Philips North America Llc

Recalled Item: The Allura Xper series is intended for use on human Recalled by Philips...

The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2021· AMTEC SALES Inc

Recalled Item: EcoGel 100 Imaging Gel Recalled by AMTEC SALES Inc Due to Ultrasound gels...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 11, 2021· Red Medical Supplies

Recalled Item: EcoGel 200 - RED Medical Supplies Blue Ultrasound Gel Recalled by Red...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 11, 2021· Red Medical Supplies

Recalled Item: EcoGel 200 - RED Medical Supplies Clear Ultrasound Gel Recalled by Red...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 11, 2021· Red Medical Supplies

Recalled Item: EcoGel 100 - RED Medical Supplies Green Ultrasound Gel Recalled by Red...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing