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. 2,542 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,542 in last 12 months

Showing 62016220 of 48,326 recalls

Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Mojo 2 Full Face AAV Non Vented Mask Recalled by SleepNet Corporation Due to...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: iQ 2 Nasal Vented Mask Recalled by SleepNet Corporation Due to Update to...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Mojo 2 Full Face Non Vented Mask Recalled by SleepNet Corporation Due to...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Mojo Non Vented Full Face Mask with Headgear Recalled by SleepNet...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Mojo 2 Full Face Vented Mask Recalled by SleepNet Corporation Due to Update...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Phantom 2 Nasal Vented Mask Recalled by SleepNet Corporation Due to Update...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· SleepNet Corporation

Recalled Item: Mojo Full Face with Headgear Recalled by SleepNet Corporation Due to Update...

The Issue: Update to contraindications and warning language due to CPAP masks...

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

Class I — Serious Health HazardOngoing
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Floaters Relief Recalled by Optikem International, Inc. Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Allergy Eyes Relief Recalled by Optikem International, Inc....

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Pink Eye Relief Recalled by Optikem International, Inc. Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Aging Eye Relief Recalled by Optikem International, Inc....

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Eye strain Relief Recalled by Optikem International, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Red Eye Relief Recalled by Optikem International, Inc. Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Eye Twitching Relief Recalled by Optikem International, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Blur Relief Recalled by Optikem International, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: TRP Natural Eyes Dryness Relief Recalled by Optikem International, Inc. Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 29, 2024· Optikem International, Inc.

Recalled Item: hyalogic For Dry Eyes Recalled by Optikem International, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 29, 2024· Beckman Coulter, Inc.

Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer is a discrete Recalled...

The Issue: The reason for the recall is the pneumatic tubing used in the analytical...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 29, 2024· Becton Dickinson & Co.

Recalled Item: BD Phoenix Yeast ID Panel is a self-inoculating (when used Recalled by...

The Issue: Esculin, a substrate used in other panels and normally in A16 well, was...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 29, 2024· Becton Dickinson & Co.

Recalled Item: BD Phoenix NMIC-306 Panel is a self-inoculating (when used with Recalled by...

The Issue: Products were found to have confirmed drug cross contamination prior to...

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

Class II — Potential Health HazardOngoing