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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19.09.2024 |
Urgent Field Safety Notice for Recharger Kit by Medtronic Inc
Product group Active implantable medical devices -
biostimulators
|
18.09.2024 |
Urgent Field Safety Notice for Visit smoke alarm optical by Bellman & Symfon Group AB
Product group General equipment for medical treatment -
furnishings
|
18.09.2024 |
Urgent Field Safety Notice for BodyGuard infusion pumps by Caesarea Medical Electronics Ltd.
Product group Injections / Infusions / Transfusions / Dialysis -
infusion technology
|
18.09.2024 |
Urgent Field Safety Notice for VARIPULSE Bi-Directional Catheter by Biosense Webster Inc
Product group Injections / Infusions / Transfusions / Dialysis -
catheters
|
16.09.2024 |
Urgent Field Safety Notice for StealthStation S. Navigation by Medtronic Navigation Inc.
Product group Radiological technology -
navigation systems
|
16.09.2024 |
Urgent Field Safety Notice for SCORE femoral component PCL sacrificing - cemented by Amplitude S.A.S.
Product group Non-active implants -
bone surgery
|
13.09.2024 |
Urgent Field Safety Notice for LIFE 21 apheresis unit by Miltenyi Biotec GmbH
Product group Injections / Infusions / Transfusions / Dialysis -
therapeutic apheresis procedures
|
13.09.2024 |
Urgent Field Safety Notice for APC (Schneider Electric IT Corporation) UPS by Philips Medical Systems
Product group Medical electronics / Electromedical devices -
electrodiagnostics
|
13.09.2024 |
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
|
13.09.2024 |
Urgent Field Safety Notice for FastPack TSH Calibrator Kit by Qualigen Inc.
Product group In-vitro diagnostics -
immunological products
|