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. 2,568 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,568 in last 12 months

Showing 32013220 of 27,852 recalls

Medical DeviceAugust 5, 2024· QUANTUM SURGICAL SAS

Recalled Item: The EPIONE device v1.0.2 is a user controlled Recalled by QUANTUM SURGICAL...

The Issue: Quantum Surgical has become aware that a component (central axis) inside the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2024· Abiomed, Inc.

Recalled Item: Pump 381 Pump Set (US) Recalled by Abiomed, Inc. Due to A potential device...

The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2024· Bard Peripheral Vascular Inc

Recalled Item: BARD MAGNUM Disposable Core Tissue Biopsy Needle MN Recalled by Bard...

The Issue: Due to possible packaging damage (indentations/cuts) cause by manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2024· AURIS HEALTH INC

Recalled Item: Monarch Platform (Endoscopy) Recalled by AURIS HEALTH INC Due to...

The Issue: Endoscopy/bronchoscopy/urology devices may have a strain relief defect with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2024· AURIS HEALTH INC

Recalled Item: Monarch Platform (Urology) Recalled by AURIS HEALTH INC Due to...

The Issue: Endoscopy/bronchoscopy/urology devices may have a strain relief defect with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX FC ESO STENT RMV 18X153MM-Wallflex Esophageal Partially Covered...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Becton Dickinson & Co.

Recalled Item: BD Phoenix 100-Intended for the rapid identification (ID) and antimicrobial...

The Issue: Escherichia coli (E. coli) misidentification for clinical samples that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: AGILE ESO FC RMV 23MM X 15.0CM IN 18.5 F- Recalled by Boston Scientific...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: AGILE ESO OTW PC 23MM X 12.0CM IN 18.5 F-Agile Recalled by Boston Scientific...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: AGILE ESO OTW FC 23MM X 10.1CM IN 18.5 F-Agile Recalled by Boston Scientific...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX PC ESOPH STENT 23/28MM X 155MM- Wallflex Esophageal Partially...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: AGILE ESO OTW FC 23MM X 15.0CM IN 18.5 F-Agile Recalled by Boston Scientific...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX ESOPHAGEAL FC 18/23-25MMX10CM- Wallflex Esophageal Partially...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX FC ESO STENT RMV LL 18X103- Wallflex Esophageal Partially Recalled...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: AGILE ESO OTW PC 23MM X 6.2CM IN 18.5 FR- Recalled by Boston Scientific...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX PC ESOPH STENT 18/23MM X 153MM- Wallflex Esophageal Partially...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX FC ESO STENT RMV LL 23X105- Intended for maintaining Recalled by...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX PC ESOPH STENT 23/28MM X 105MM- Wallflex Esophageal Partially...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX ESOPHAGEAL FC 23/28MMX12CM- Wallflex Esophageal Partially Covered...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2024· Boston Scientific Corporation

Recalled Item: WALLFLEX ESOPHAGEAL FC 18/23-25MMX15CM- Agile Esophageal Partially Covered...

The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...

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

Class II — Potential Health HazardOngoing