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. 2,498 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,498 in last 12 months

Showing 1250112520 of 27,852 recalls

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
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
Medical DeviceNovember 19, 2019· Angiodynamics, Inc.

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

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 EXTERNAL BEAM PHOTON Recalled by Angiodynamics, Inc. Due to May...

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 18, 2019· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation stand-alone software treatment planning system Recalled by...

The Issue: Editing a static arc beam may unexpectedly set the MU of the beam to its...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2019· Diagnostica Stago, Inc.

Recalled Item: STA SYSTEM CONROL N + P (ref. 00678) Recalled by Diagnostica Stago, Inc. Due...

The Issue: A positive bias was confirmed to exists on the STA - Unicalibrator levels...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2019· Diagnostica Stago, Inc.

Recalled Item: STA UNICALIBRATOR (ref. 00675) Recalled by Diagnostica Stago, Inc. Due to A...

The Issue: A positive bias was confirmed to exists on the STA - Unicalibrator levels...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2019· Leica Microsystems, Inc.

Recalled Item: BOND Polymer Detection Kit Recalled by Leica Microsystems, Inc. Due to BOND...

The Issue: BOND Polymer Detection kits (DS9800) were held out of storage longer than...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2019· Boston Scientific Corporation

Recalled Item: Habib EUS RFA Recalled by Boston Scientific Corporation Due to During...

The Issue: During testing on the Habib EUS RFA device, a temperature increase was...

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

Class II — Potential Health HazardOngoing