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. 2,400 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,400 in last 12 months

Showing 2242122440 of 48,326 recalls

Medical DeviceMarch 13, 2019· Exactech, Inc.

Recalled Item: Truliant Tibial Fit Tray Cemented SZ 3F / 3T Recalled by Exactech, Inc. Due...

The Issue: 2.5 Truliant Fit Trays were mismarked as 3

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

Class II — Potential Health HazardOngoing
DrugMarch 12, 2019· MSM Nutraceuticals, LLC

Recalled Item: Red Eye Recalled by MSM Nutraceuticals, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Product is not terminally sterialized and...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 12, 2019· MSM Nutraceuticals, LLC

Recalled Item: Dry Eye Recalled by MSM Nutraceuticals, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Product is not terminally sterialized and...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 12, 2019· MSM Nutraceuticals, LLC

Recalled Item: Dr. Berne's MSM DROPS 15% Solution Recalled by MSM Nutraceuticals, LLC Due...

The Issue: Lack of Assurance of Sterility: Product is not terminally sterialized and...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 12, 2019· MSM Nutraceuticals, LLC

Recalled Item: 15% MSM Recalled by MSM Nutraceuticals, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Product is not terminally sterialized and...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 12, 2019· Akorn Inc

Recalled Item: Hydrocortisone and Acetic Acid Otic Solution Recalled by Akorn Inc Due to...

The Issue: Sub Potent Drug: OOS results observed for the Hydrocortisone assay during...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 12, 2019· Ethicon, Inc.

Recalled Item: PDS II SUTURE 18"(45CM) 2-0 VIO Product Code:Z739D - PDS Recalled by...

The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2019· Ethicon, Inc.

Recalled Item: VICRYL PLUS Sutures: VICRYL PLUS SUTURE 18"(45CM) 3-0 VIO VICRYL Recalled by...

The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2019· Ethicon, Inc.

Recalled Item: VICRYL Sutures VICRYL SUTURE 18"(45CM) 0 VIO VICRYL SUTURE 18"(45CM)...

The Issue: VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2019· Elekta Limited

Recalled Item: Elekta Unity Recalled by Elekta Limited Due to Users need to be aware when...

The Issue: Users need to be aware when using these protocols for daily on line plan...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2019· Beaver Visitec

Recalled Item: Beaver Xstar Slit Knife 2.4 mm Recalled by Beaver Visitec Due to Mislabeling

The Issue: Mislabeled. The package labeling indicates a size 2.4mm, 45 degree Double...

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

Class II — Potential Health HazardOngoing
DrugMarch 11, 2019· Teva Pharmaceuticals USA

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets Recalled by Teva...

The Issue: Subpotent Drug.

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 11, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics Due...

The Issue: One of the software algorithms used to detect sample dispense errors was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2019· Brainlab AG

Recalled Item: RT Elements Software revisions of the RT Elements applications have Recalled...

The Issue: There is a potential for an incorrect dose distribution calculation by...

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

Class II — Potential Health HazardOngoing
FoodMarch 8, 2019· Hometown Food Company

Recalled Item: Pillsbury Unbleached All Purpose Flour Enriched 5Lb paper bag retail....

The Issue: Product may be contaminated with Salmonella

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

Recalled Item: Salto Talaris Tibial Total Ankle Prosthesis Tray Recalled by Integra...

The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

Recalled Item: Talar Dome Total Ankle Prosthesis Recalled by Integra LifeSciences Corp. Due...

The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

Recalled Item: Salto Talaris Tibial Ankle Prosthesis Tray Recalled by Integra LifeSciences...

The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

Recalled Item: Talar Dome Total Ankle Prosthesis Recalled by Integra LifeSciences Corp. Due...

The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...

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

Class II — Potential Health HazardOngoing