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. 2,548 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,548 in last 12 months

Showing 53015320 of 48,326 recalls

DrugMay 24, 2024· SYNCHRONICITY SPA INC, DBA SUNTE

Recalled Item: suntegrity Recalled by SYNCHRONICITY SPA INC, DBA SUNTE Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: Presence of Aspergillus...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 24, 2024· CUE HEALTH INC

Recalled Item: Cue Health COVID-19 Test Cartridge Cue COVID-19 Test Recalled by CUE HEALTH...

The Issue: Due to modified test kits being marketed and distributed without FDA...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2024· WOM World Of Medicine AG

Recalled Item: WOM Tube Set for lrrlgatlon Recalled by WOM World Of Medicine AG Due to...

The Issue: Incorrect transponder data was written on the RFID tags triggers the error...

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

Class II — Potential Health HazardOngoing
DrugMay 23, 2024· Eugia US LLC

Recalled Item: Dexamethasone Sodium Phosphate injection USP Recalled by Eugia US LLC Due to...

The Issue: Failed Impurities/Degradation Specifications: impurity sulfonic acid adduct...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 23, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zoledronic Acid Injection 5mg/100mL Sterile Solution Recalled by Dr. Reddy's...

The Issue: Lack of Assurance of Sterility: Leaking vials

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 23, 2024· Alcon Research LLC

Recalled Item: Surgical Image Guidance Functionality Recalled by Alcon Research LLC Due to...

The Issue: After surgery initiation, while using surgical image guidance, if...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2024· Howmedica Osteonics Corp.

Recalled Item: Gray Revision Instrument System Accessory Tray/Case Recalled by Howmedica...

The Issue: The design of the HRIS Storage & Sterilization Case and Tray P/N 6210-9-900...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2024· Howmedica Osteonics Corp.

Recalled Item: HRIS Storage & Sterilization Case and Tray Recalled by Howmedica Osteonics...

The Issue: The design of the HRIS Storage & Sterilization Case and Tray P/N 6210-9-900...

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

Class II — Potential Health HazardOngoing
DrugMay 22, 2024· MexHealth LLC

Recalled Item: OSSOS-SANS con: Glucosamina Curcuma Ortiga tablets Recalled by MexHealth LLC...

The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2024· Eugia US LLC

Recalled Item: Eptifibatide injection 20mg/10mL (2mg/mL) Recalled by Eugia US LLC Due to...

The Issue: Failed Impurities/Degradation Specifications: failed related substance...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 22, 2024· Beckman Coulter, Inc.

Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...

The Issue: When a DxI 9000 Access Immunoassay Analyzer is connected to a Laboratory...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2024· Beckman Coulter, Inc.

Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer Recalled by Beckman...

The Issue: The reason for this recall is Beckman Coulter has determined that when a DxI...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2024· Abbott Medical

Recalled Item: Abbott Infinity 5 Recalled by Abbott Medical Due to Their is a potential...

The Issue: Their is a potential that the implantable pulse generator replacement...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2024· Abbott Medical

Recalled Item: Abbott Infinity 7 Recalled by Abbott Medical Due to Their is a potential...

The Issue: Their is a potential that the implantable pulse generator replacement...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2024· Abbott Medical

Recalled Item: Abbott Infinity 5 Recalled by Abbott Medical Due to Their is a potential...

The Issue: Their is a potential that the implantable pulse generator replacement...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2024· Abbott Medical

Recalled Item: Abbott Infinity 7 Recalled by Abbott Medical Due to Their is a potential...

The Issue: Their is a potential that the implantable pulse generator replacement...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2024· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Endo Model SL Tibial Components 16-2817/02 Tibial Component Recalled by...

The Issue: Blind screws of the modular tibial component cannot be loosened...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2024· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: Endo Model M Tibial Components Modular Knee Prosthesis System. Product...

The Issue: Blind screws of the modular tibial component cannot be loosened...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2024· Philips North America Llc

Recalled Item: Avalon Ultrasound Transducer. Directs low-energy ultrasound beam toward the...

The Issue: Potential for inaccurate fetal heart rate measurements when monitoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2024· Thoratec Switzerland GMBH

Recalled Item: 2nd Generation CentriMag Primary Console Recalled by Thoratec Switzerland...

The Issue: Due to a component change, the console part of a circulatory support system...

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

Class II — Potential Health HazardOngoing