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. 2,548 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,548 in last 12 months

Showing 52815300 of 27,852 recalls

Medical DeviceOctober 19, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: epoc NXS Host Blood Analysis System Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed a potential issue that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra¿ Cranial Access Kit-For access to the subarachnoid space or Recalled...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra¿ Cranial Access Kit-For access to the subarachnoid space or Recalled...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Abbott Laboratories

Recalled Item: Alinity i Processing Module The Alinity i Processing Recalled by Abbott...

The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit-For access to the subarachnoid space or Recalled...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Abbott Laboratories

Recalled Item: Alinity c Processing Module The Alinity c Processing Recalled by Abbott...

The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Combo Kit Consists OF 10-110/INS-4500/INS-7040- For access to the...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial access kit (without Prep solutions) Bit and Guard-For...

The Issue: Defect in the outer packaging of the Cranial Access Kits can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Meridian Bioscience Inc

Recalled Item: Cardinal Health Clean Stool Transportation System-For the collection...

The Issue: Due to a manufacturing defect, certain Para-Pak vials may be at risk for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit - For access to the subarachnoid Recalled by...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit- For access to the subarachnoid space Recalled by...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Meridian Bioscience Inc

Recalled Item: Para-Pak Zn-PVA/10% Formalin-for the routine collection Recalled by Meridian...

The Issue: Plastic vials contain a manufacturing defect may cause an increased risk of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit -For access to the subarachnoid space Recalled by...

The Issue: Defect in the outer packaging of the Cranial Access Kits can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Abbott Laboratories

Recalled Item: ARCHITECT c4000 Processing Module 02P24-02 02P24-40 01R24-56 01R25-56...

The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2023· Integra LifeSciences Corp.

Recalled Item: Integra Cranial Access Kit-For access to the subarachnoid space or Recalled...

The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· Microbiologics Inc

Recalled Item: KWIKSTIK Recalled by Microbiologics Inc Due to A complaint investigation...

The Issue: A complaint investigation showed that the bulk pellets (lot 794-142) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· AURIS HEALTH INC

Recalled Item: Monarch Platform Recalled by AURIS HEALTH INC Due to Their is the potential...

The Issue: Their is the potential that software issues may result in flipped image of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· Microbiologics Inc

Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to A complaint investigation...

The Issue: A complaint investigation showed that the bulk pellets (lot 794-142) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· AURIS HEALTH INC

Recalled Item: Monarch Platform Recalled by AURIS HEALTH INC Due to Their is the potential...

The Issue: Their is the potential that software issues may result in flipped image of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· AURIS HEALTH INC

Recalled Item: Monarch Platform 100-240V- 50/60Hz 1440w Recalled by AURIS HEALTH INC Due to...

The Issue: Their is the potential that software issues may result in flipped image of...

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

Class II — Potential Health HazardOngoing