Field Corrective Actions
Field Corrective Actions include removals of medical devices from the market or any other corrective action on devices in use. In general, the manufacturer implements field corrective actions by sending an advisory notice to inform operators and users about risks of medical devices, and to advise on what action should be taken to protect the health or the safety of patients, users or other persons. For example, advisory notices may contain the information from the manufacturer that he voluntarily recalls a medical device. Please note that advisory notices are issued by the manufacturer, the authorized representative or the importer of medical devices. The respective company takes the responsibility for all information given in the advisory notice.
RSS-Feed of Field Corrective Actions.
After clicking on the button "find all field corrective actions" all customer information can be searched and additionally filtered by product groups.
find all field corrective actions
Date | Title: |
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16.09.2025 |
Urgent Field Safety Notice for Magnet Venting Path of 3 Tesla MRI System by Siemens Shenzhen Magnetic Resonance Ltd.
Product group Electromedical fields -
equipment for MR tomography
|
16.09.2025 |
Urgent Field Safety Notice for Heater Unit HU35 by Maquet Cardiopulmonary AG
Product group Surgical equipment/ Anaesthesia -
surgical equipment
|
16.09.2025 |
Urgent Field Safety Notice for Sharesource Claria Connectivity Platform (Product Code 5CGM01 by Baxter Healthcare S. (Opfikon)
Product group Injections / Infusions / Transfusions / Dialysis -
dialysis technology
|
15.09.2025 |
Urgent Field Safety Notice for FreeStyle Libre 3 Plus by Abbott Diabetes Care Ltd. UK
Product group Medical electronics / Electromedical devices -
electric blood glucose meters
|
12.09.2025 |
Urgent Field Safety Notice for MassCheck Dried Blood Spot Control Bi-Level I+II by Chromsystems Instruments & Chemicals GmbH
Product group In-vitro diagnostics -
equipment / products for clinical chemistry
|
12.09.2025 |
Urgent Field Safety Notice for Charging unit mounted W/T AC TS7500 by Baxter Medical Systems GmbH + Co. KG
Product group Surgical equipment/ Anaesthesia -
surgical equipment
|
12.09.2025 |
Urgent Field Safety Notice for STA LIATEST DDI PLUS (IVDR Class C) by Diagnostica Stago
Product group In-vitro diagnostics -
haematological, histological and cytological products
|
12.09.2025 |
Urgent Field Safety Notice for RENZAN by MicroVention,INC.
Product group Non-active implants -
special implants
|
11.09.2025 |
Urgent Field Safety Notice for Allura Xper, Allura CV20 by Philips Nordic
Product group Radiological technology -
radiological equipment for vascular diagnostics
|
10.09.2025 |
Urgent Field Safety Notice for Getinge 88-series by Getinge Disinfection AB
Product group General equipment for medical treatment -
cleaning / disinfection / sterilisation
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