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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02.09.2025 |
Urgent Field Safety Notice for Swelab Alfa Plus; Medonic M-Series M32 by Boule Medical AB (Spånga)
Product group In-vitro diagnostics -
haematological, histological and cytological products
|
02.09.2025 |
Urgent Field Safety Notice for AeroWalk Carbon Rollator by Drive Medical GmbH & Co. KG
Product group Orthopaedic / Rehabilitation technology -
daily living aids
|
02.09.2025 |
Urgent Field Safety Notice for HistoCore PELORIS 3 by Leica Biosystems Melbourne Pty Ltd
Product group In-vitro diagnostics -
instruments, apparatuses and systems
|
01.09.2025 |
Urgent Field Safety Notice for PIXIUM PORTABLE 4343 EZ-C X by THALES AVS FRANCE SAS
Product group Radiological technology -
mobile radiological diagnostic facilities
|
01.09.2025 |
Urgent Field Safety Notice for STRYKEFLOW2 by Stryker Endoscopy-San Jose
Product group Optics / Precision engineering -
endoscopes
|
01.09.2025 |
Urgent Field Safety Notice for Drive complete PSP, green claws by B.Braun Melsungen AG
Product group Injections / Infusions / Transfusions / Dialysis -
infusion technology
|
01.09.2025 |
Urgent Field Safety Notice for REUSABLE TROCAR SYSTEM 10MM, 12MM by Aesculap AG
Product group Medical instruments for use in humans -
visceral surgery
|
29.08.2025 |
Urgent Field Safety Notice for Option Rhinomanometry, Option SNIP by Jaeger Medical GmbH
Product group Medical electronics / Electromedical devices -
pulmonary function diagnostics
|
29.08.2025 |
Urgent Field Safety Notice for FIAB electrodes for external defibrillation by FIAB SpA
Product group Medical electronics / Electromedical devices -
electrotherapy
|
29.08.2025 |
Urgent Field Safety Notice for Elefant Suction/irrigation device by Coloplast A/S
Product group Optics / Precision engineering -
endoscopes
|