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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24.04.2025 |
Urgent Field Safety Notice for CARDIOHELP System by Maquet Cardiopulmonary AG
Product group Surgical equipment/ Anaesthesia -
surgical equipment
|
23.04.2025 |
Urgent Field Safety Notice for OTNI 17 Luci Connector by OTN Innovations B.V
Product group Orthopaedic / Rehabilitation technology -
prostheses (exoprostheses)
|
23.04.2025 |
Urgent Field Safety Notice for VasoView Hemopro 2 by Maquet Cardiovascular
Product group Optics / Precision engineering -
endoscopes
|
23.04.2025 |
Urgent Field Safety Notice for GOT Multi (SF6, C2F6, C3F8) by AL.CHI.MI.A. S.R.L.
Product group ophthalmological technology -
liquid media for ophthalmological purposes
|
23.04.2025 |
Urgent Field Safety Notice for Eye wick by GRI Medical & Electronic Technology Co., Ltd.
Product group Dressings / Pads -
swabs, sponges, wipes, swabsticks
|
23.04.2025 |
Urgent Field Safety Notice for Soltive Laser System by Gyrus ACMI, Inc.
Product group Optics / Precision engineering -
laser technology
|
22.04.2025 |
Urgent Field Safety Notice for Xpert BCR/ABL Ultra, Xpert BCR/ABL Ultra p190 by Cepheid
Product group In-vitro diagnostics -
immunological products
|
17.04.2025 |
Urgent Field Safety Notice for Tornado Embolization MicrocoilT by Cook Incorporated
Product group Non-active implants -
special implants
|
17.04.2025 |
Urgent Field Safety Notice for Centricity High Acuity (CHA) C.C and Anesthesia by GE Healthcare Finland Oy
Product group Medical electronics / Electromedical devices -
electrodiagnostics
|
17.04.2025 |
Urgent Field Safety Notice for Mecta-C Stand Alone screws by Medacta International SA
Product group Non-active implants -
bone surgery
|