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. 2,535 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,535 in last 12 months

Showing 69216940 of 48,326 recalls

Medical DeviceNovember 30, 2023· Philips North America Llc

Recalled Item: Spectral CT 7500 Recalled by Philips North America Llc Due to Multiple...

The Issue: Multiple software issues that affect device functionality.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2023· Philips North America

Recalled Item: BrightView X Recalled by Philips North America Due to While using...

The Issue: While using Pre-Programmed Motion during an extrinsic quality assurance...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2023· Philips North America

Recalled Item: BrightView Recalled by Philips North America Due to While using...

The Issue: While using Pre-Programmed Motion during an extrinsic quality assurance...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2023· Philips North America

Recalled Item: BrightView XCT Recalled by Philips North America Due to While using...

The Issue: While using Pre-Programmed Motion during an extrinsic quality assurance...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2023· Boston Scientific Corporation

Recalled Item: Boston Scientific Model 3120 ZOOM LATITUDE Programmer/Recorder/Monitor (PRM)...

The Issue: The software application on the Programmer/Recorder/Monitor (PRM) for...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2023· Insulet Corporation

Recalled Item: Omnipod 5 App (on compatible Android smartphones) Recalled by Insulet...

The Issue: The bolus calculator is not recording the decimal point if it is the first...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 30, 2023· Busse Hospital Disposables, Inc.

Recalled Item: Catalog No. 9251R1 Recalled by Busse Hospital Disposables, Inc. Due to Firm...

The Issue: Firm is recalling all kits containing recalled lots of Nurse Assist Sterile...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 30, 2023· Busse Hospital Disposables, Inc.

Recalled Item: Catalog No. 1443 DRESSING CHANGE TRAY / STERILE - LATEX FREE Recalled by...

The Issue: Firm is recalling all kits containing recalled lots of Nurse Assist Sterile...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 30, 2023· Busse Hospital Disposables, Inc.

Recalled Item: Catalog No. 800 TRACHEOSTOMY CARE TRAY - STERILE -LATEX FREE Recalled by...

The Issue: Firm is recalling all kits containing recalled lots of Nurse Assist Sterile...

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

Class I — Serious Health HazardOngoing
DrugNovember 29, 2023· Meta Herbal

Recalled Item: Magnum XXL 9800 Recalled by Meta Herbal Due to Undeclared Active

The Issue: Marketed without an approved NDA/ANDA: Magnum XXL found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 29, 2023· STAQ Pharma, Inc.

Recalled Item: ROPivacaine HCl 0.2% PF in Sodium Chloride 1 Recalled by STAQ Pharma, Inc....

The Issue: STAQ Pharma Inc. received consumer complaints related to leaking bags and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 29, 2023· Randox Laboratories Ltd.

Recalled Item: RX Series Copper (Cu) Assay Ref. Number CU2340 Recalled by Randox...

The Issue: Randox Laboratories have released an update to the Carryover Avoidance...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2023· American Contract Systems, Inc.

Recalled Item: Procedural convenience kits and trays Recalled by American Contract Systems,...

The Issue: During an internal investigation, ACS identified that several components...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2023· American Contract Systems, Inc.

Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...

The Issue: During an internal investigation, ACS identified that several components...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2023· American Contract Systems, Inc.

Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...

The Issue: During an internal investigation, ACS identified that several components...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2023· American Contract Systems, Inc.

Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...

The Issue: During an internal investigation, ACS identified that several components...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2023· American Contract Systems, Inc.

Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...

The Issue: During an internal investigation, ACS identified that several components...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2023· American Contract Systems, Inc.

Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...

The Issue: During an internal investigation, ACS identified that several components...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2023· American Contract Systems, Inc.

Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...

The Issue: During an internal investigation, ACS identified that several components...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2023· American Contract Systems, Inc.

Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...

The Issue: During an internal investigation, ACS identified that several components...

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

Class II — Potential Health HazardOngoing