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. 2,443 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,443 in last 12 months

Showing 1938119400 of 48,326 recalls

DrugNovember 20, 2019· Idelle Labs

Recalled Item: SURE 48hr Confidence Regular Original Solid Anti-Perspirant & Deodorant Net...

The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2019· Idelle Labs

Recalled Item: SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant &...

The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2019· Idelle Labs

Recalled Item: SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant...

The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2019· AuroMedics Pharma LLC

Recalled Item: Mirtazapine Tablets Recalled by AuroMedics Pharma LLC Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 20, 2019· AuroMedics Pharma LLC

Recalled Item: Mirtazapine Tablets Recalled by AuroMedics Pharma LLC Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Outlook Safety Infusion System Y-type Blood Set Recalled by B. Braun...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
DrugNovember 19, 2019· AuroMedics Pharma LLC

Recalled Item: Gabapentin Capsules Recalled by AuroMedics Pharma LLC Due to Presence of...

The Issue: Presence of Foreign Tablets/Capsules: One Losartan/HCTZ tablet was found in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 19, 2019· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Irrigation USP 5000 mL bags Recalled by Baxter...

The Issue: Lack of Assurance of Sterility: Product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 19, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry CardioPhase High Sensitivity C-Reactive Protein (hsCRP)...

The Issue: Atellica and ADVIA hsCRP calibrator accuracy has drifted away from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH High Sensitivity C-Reactive Protein (HsCRP) Calibrator - Product...

The Issue: Atellica CH: The Atellica¿ CH High Sensitivity CReactive Protein Calibrator...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Cardiac Assist, Inc

Recalled Item: TandemLife ECLS Procedure Kit - V24/A17 Recalled by Cardiac Assist, Inc Due...

The Issue: The kit contained a 29Fr ProtekDuo cannula instead of a 24Fr Protek Solo...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Angiodynamics, Inc.

Recalled Item: OARTRAC PROSTATE IMMOBILIZATION ENDORECTAL BALLOON DEVICE KIT Recalled by...

The Issue: May result in readings outside of the expected accuracy range.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Angiodynamics, Inc.

Recalled Item: OARtrac PLUS CLINICAL DETECTOR UNIT Catalog Number: OTS-V2-Plus - Product...

The Issue: May result in readings outside of the expected accuracy range.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Angiodynamics, Inc.

Recalled Item: MICRO-PSD HDR Recalled by Angiodynamics, Inc. Due to May result in readings...

The Issue: May result in readings outside of the expected accuracy range.

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

Class II — Potential Health HazardOngoing