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. 2,535 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,535 in last 12 months

Showing 68416860 of 27,852 recalls

Medical DeviceJanuary 16, 2023· Siemens Medical Solutions USA, Inc.

Recalled Item: SIEMENS Biograph Horizon 3R Mobile Recalled by Siemens Medical Solutions...

The Issue: This is a potential problem with the locking mechanism that is used to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Folate 140 test kit- For in vitro diagnostic Recalled by Siemens...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Folate 700 test kit (REF)-For in vitro diagnostic Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Folate 100 test kit-For in vitro diagnostic use Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Folate 700 test kit- For in vitro diagnostic Recalled by Siemens...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Folate 500 test kit (REF)-For in vitro diagnostic Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Folate 500 test kit- For in vitro diagnostic Recalled by...

The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2023· S & MOHR AMERICA, S.A. DE C.V.

Recalled Item: abm Respiratory Care Standart Breating Circuit with Face Mask - Recalled by...

The Issue: Incorrect expiration date on product label. The manufacturing date was...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 4, 2023· Wishbone Medical, Inc.

Recalled Item: WishBone Medical Smart Correction Dual Joint Express Struts Recalled by...

The Issue: Firm identified that user may be unable to adjust the length of the Smart...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2023· Bard Peripheral Vascular Inc

Recalled Item: Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter...

The Issue: Due to the adhesive provided within the catheter repair kits maybe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2023· Western/Scott Fetzer Company

Recalled Item: Digital VIPR ROC-9839 Roberts Oxygen Ready to Use Digital VIPR Recalled by...

The Issue: Gauge malfunction: Digital gauge displays an incorrect tank pressure -...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Medline Sterile Hand Pack Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: The convenience trays had improper placement of some of the components that...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Sterile Oncology Port Access Tray Recalled by MEDLINE INDUSTRIES, LP...

The Issue: The convenience trays had improper placement of some of the components that...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Medline Sterile Maximum Barrier Pack-LF Recalled by MEDLINE INDUSTRIES,...

The Issue: The convenience trays had improper placement of some of the components that...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2022· Philips Healthcare (Suzhou) Co., Ltd.

Recalled Item: Incisive CT Recalled by Philips Healthcare (Suzhou) Co., Ltd. Due to...

The Issue: Multiple software issues which have the potential to lead to misdiagnosis...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2022· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LinkSymphoKnee Distal Femoral Augment - Tilastan - Size. 7-8 Recalled by...

The Issue: Fixation screw was inserted through the wrong side of the augment (distal to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2022· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LinkSymphoKnee Distal Femoral Augment - Tilastan - Size 7-8 Recalled by...

The Issue: Fixation screw was inserted through the wrong side of the augment (distal to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2022· Quest Medical, Inc.

Recalled Item: Precision Delivery Set with Filter Recalled by Quest Medical, Inc. Due to...

The Issue: Delivery Sets may have tubing that could become detached that could result...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CENTURION MEDICAL PRODUCTS Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: The kit contained an expired component.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2022· Access Vascular, Inc

Recalled Item: HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short Recalled...

The Issue: Product Mislabeled on the outer bag and inner kit Tyvek header bag

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

Class II — Potential Health HazardOngoing