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. 2,526 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,526 in last 12 months

Showing 1028110300 of 48,326 recalls

Medical DeviceNovember 29, 2022· Biomet, Inc.

Recalled Item: OSS Modular Arthrodesis Nail Recalled by Biomet, Inc. Due to Product missing...

The Issue: Product missing the four small locking collar bolts resulting in extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2022· Acumed LLC

Recalled Item: Acutrak 2 Part Number/Part Description: 30-0021 25.0mm Acutrak 2¿ - Recalled...

The Issue: Distribution without Pre-Market Clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2022· Acumed LLC

Recalled Item: Dual-Trak Clavicle Screws Part Number/Part Description: 40-0136 3.0mm x 80mm...

The Issue: Distribution without Pre-Market Clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2022· Acumed LLC

Recalled Item: AcuTwist Acutrak Compression Screws Part Number/Part Description: AI-0010-S...

The Issue: Distribution without Pre-Market Clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2022· Acumed LLC

Recalled Item: Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose...

The Issue: Distribution without Pre-Market Clearance

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

Class II — Potential Health HazardOngoing
DrugNovember 28, 2022· Exela Pharma Sciences LLC

Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...

The Issue: Defective Container: Complaints received of vial breakage and glass flying...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 28, 2022· Exela Pharma Sciences LLC

Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...

The Issue: Defective Container: Complaints received of vial breakage and glass flying...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 28, 2022· Rocky Mountain Pies, LLC

Recalled Item: Red Button Vintage Creamery French Silk Pie Recalled by Rocky Mountain Pies,...

The Issue: Pies labeled as Red Button French Silk may contain Turtle Cream Pies...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 28, 2022· Universal Meditech Inc.

Recalled Item: Products are labeled as: Skippack Medical Lab SARS-CoV-2 Antigen Rapid...

The Issue: Distribution of SARS-CoV-2 Antigen Rapid Test Kits without FDA market...

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

Class I — Serious Health HazardOngoing
DrugNovember 23, 2022· Heritage Pharmaceuticals Inc

Recalled Item: Desmopressin Acetate Tablets 0.2mg Recalled by Heritage Pharmaceuticals Inc...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos Agile Max (VE10 Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos dRF Max (VE10 Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: LUMINOS Lotus Max (VF11) Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Baxter Healthcare Corporation

Recalled Item: Revaclear 300 dialyzers. Indicated for treatment of chronic and acute...

The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Baxter Healthcare Corporation

Recalled Item: Revaclear 400 dialyzers. Indicated for treatment of chronic and acute...

The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Baxter Healthcare Corporation

Recalled Item: Revaclear 400 Dialyzer. Product Code: 114749M. Not distributed in the...

The Issue: Potential for Internal Blood Leaks due to a twisted gasket in the dialyzer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Baxter Healthcare Corporation

Recalled Item: Revaclear 400 Dialyzer. Product Code: 114746L. Used to treat chronic...

The Issue: Potential for Internal Blood Leaks due to a twisted gasket in the dialyzer

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 23, 2022· Baxter Healthcare Corporation

Recalled Item: Revaclear 400 dialyzers. Indicated for treatment of chronic and acute...

The Issue: Reports of Polyurethane Displacement in the dialyzer, and might be...

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

Class II — Potential Health HazardOngoing
DrugNovember 22, 2022· Fresenius Kabi USA, LLC

Recalled Item: Sensorcaine (Bupivacaine HCl and Epinephrine Injection Recalled by Fresenius...

The Issue: Subpotent Drug: Testing results below the defined limit for the epinephrine...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 22, 2022· Fresenius Kabi USA, LLC

Recalled Item: Sensorcaine-MPF (Bupivacaine HCl and Epinephrine Injection Recalled by...

The Issue: Subpotent Drug: Testing results below the defined limit for the epinephrine...

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

Class II — Potential Health HazardOngoing
Refund