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. 2,552 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,552 in last 12 months

Showing 44414460 of 48,326 recalls

Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: basixSKY Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: MONARCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: DiamondTOUCH Digital Inflation Device Recalled by Merit Medical Systems,...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: BlueFIRE Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: Blue Diamond Digital Inflation Device Recalled by Merit Medical Systems,...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: basixTOUCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: StabiliT TOUCH Syringe Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Merit Medical Systems, Inc.

Recalled Item: IntelliSystem Inflation Device Recalled by Merit Medical Systems, Inc. Due...

The Issue: Inflation devices may have a small hole in the sterile barrier of the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2024· Hologic Inc

Recalled Item: Selenia Dimensions/ 3Dimensions-Digital breast tomosynthesis Software...

The Issue: Identified an issue with Selenia Dimensions 1.12.0 and 3Dimensions 2.3.0...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Tonsil Tray that contains the Cardinal Recalled by Windstone...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Septo Pack that contains the Cardinal Recalled by Windstone...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical T and A Pack that contains Recalled by Windstone Medical...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Tonsil Pack that contains the Cardinal Recalled by Windstone...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2024· Windstone Medical Packaging, Inc.

Recalled Item: Aligned Medical Tonsil ENT Pack that contains the Recalled by Windstone...

The Issue: Due to convenience kits containing a kit component that is under a recall...

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

Class II — Potential Health HazardOngoing
DrugAugust 15, 2024· Biocompatibles UK, Ltd.

Recalled Item: Varithena (polidocanol injectable foam) Administration Pack Recalled by...

The Issue: Defective Delivery System: incorrect silicone oil-free NormJect 10 mL Luer...

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

Class III — Low RiskOngoing
Refund
DrugAugust 15, 2024· Fagron Compounding Services

Recalled Item: Lidocaine HCl Injection Recalled by Fagron Compounding Services 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
Medical DeviceAugust 15, 2024· Roche Diagnostics Operations, Inc.

Recalled Item: Creatine Kinase (CK) used on cobas c 311/501/502 and COBAS Recalled by Roche...

The Issue: Creatine Kinase (CK) Assay Abnormal calibrations on the cobas¿ c 311/501/502...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2024· CareFusion 303, Inc.

Recalled Item: Alaris EtCO2 Module Model 8300 Recalled by CareFusion 303, Inc. Due to Due...

The Issue: Due to affected devices that may have bent female IUI connector and may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2024· B Braun Medical Inc

Recalled Item: SL BLOODLINE FOR FMC 2008 SERIES-Tubing to be used to Recalled by B Braun...

The Issue: Incomplete insertion of the patient connector of the Streamline Airless...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2024· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module Model 8100 Recalled by CareFusion 303, Inc. Due to Due to...

The Issue: Due to affected devices that may have bent female IUI connector and may not...

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

Class II — Potential Health HazardOngoing