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. 2,026 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,026 in last 12 months

Showing 33813400 of 48,326 recalls

Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Due to an increase in...

The Issue: Due to an increase in complaints for pitch cable failures related to forceps...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Due to an increase in...

The Issue: Due to an increase in complaints for pitch cable failures related to forceps...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Becton Dickinson & Co.

Recalled Item: BD PCR Cartridges used with MAX System. Model Number: 437519 Recalled by...

The Issue: Potential for signal drift in specific lots of BD PCR Cartridges.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· New Medical Technologies Gmbh

Recalled Item: Integra Miltex CryoSolutions Cartridges 10 Pack (23.5g N2O each) Recalled by...

The Issue: During the assembly of the cartridge to its connecting body part, the valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Ortho-Clinical Diagnostics, INc.

Recalled Item: Brand Name: VITROS Product Name: VITROS 5600 Integrated System Model/Catalog...

The Issue: The VITROS 5600 Integrated System software versions 3.8.0 may not correctly...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Ortho-Clinical Diagnostics, INc.

Recalled Item: Brand Name: VITROS Product Name: VITROS XT 7600 Integrated System Recalled...

The Issue: The VITROS XT 7600 Integrated System software versions 3.8.0 may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope - - Optical Biopsy and Grasping Forceps Recalled by...

The Issue: Due to failure of manual cleaning validation, biopsy and grasping forceps...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· New Medical Technologies Gmbh

Recalled Item: Integra Miltex Cryosolutions Cartridges 4 Pack (23.5g N2O each) Recalled by...

The Issue: During the assembly of the cartridge to its connecting body part, the valve...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Karl Storz Endoscopy

Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...

The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2024· Ortho-Clinical Diagnostics, INc.

Recalled Item: Brand Name: VITROS Product Name: VITROS 3600 Immunodiagnostic System...

The Issue: The VITROS 3600 Immunodiagnostic System software versions 3.8.0 may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2024· Encore Medical, LP

Recalled Item: EMPOWR 3D Knee Tibial Insert Recalled by Encore Medical, LP Due to 5R 16MM...

The Issue: 5R 16MM knee tibial insert package may contain knee tibial insert 3R 14MM...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2024· Instrumentation Laboratory

Recalled Item: HemosIL Heparin Calibrators Recalled by Instrumentation Laboratory Due to...

The Issue: Control indicating lower than expected quality control (QC) results and in...

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

Class II — Potential Health HazardOngoing