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: |
|---|---|
| 04.09.2025 |
Urgent Field Safety Notice for Automated Impella Controller by ABIOMED Inc.
Product group Medical electronics / Electromedical devices -
electrotherapy
|
| 04.09.2025 |
Urgent Field Safety Notice for ATELLICA CH / ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) by Siemens Healthcare Diagnostics Inc. Tarrytown
Product group In-vitro diagnostics -
equipment / products for clinical chemistry
|
| 04.09.2025 |
Urgent Field Safety Notice for MEDILOOPS by Neuromedex GmbH
Product group Dressings / Pads -
surgical sutures, vascular loops etc.
|
| 04.09.2025 |
Urgent Field Safety Notice for AlloSeq cfDNA Software IFU by CareDx Pty Ltd
Product group In-vitro diagnostics -
instruments, apparatuses and systems
|
| 03.09.2025 |
Urgent Field Safety Notice for Dexcom G6 CGM System by Dexcom, Inc
Product group Medical electronics / Electromedical devices -
electric blood glucose meters
|
| 03.09.2025 |
Urgent Field Safety Notice for Blue sail EndoBule Endoscopic Stapler I by Changzhou Tongchuang Medical Instrument Technology Co. Ltd.
Product group Medical instruments for use in humans -
general instruments
|
| 03.09.2025 |
Urgent Field Safety Notice for VAIOS Shoulder Modular Humeral Stem H-AC 10mm Diameter by JRI Orthopaedics Ltd.
Product group Non-active implants -
bone surgery
|
| 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
|