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: |
|---|---|
| 02.06.2025 |
Urgent Field Safety Notice for MiTF, (C5 & D5) by Bio S., Inc.
Product group In-vitro diagnostics -
equipment / products for clinical chemistry
|
| 02.06.2025 |
Urgent Field Safety Notice for Alinity i Total PSA Reagent Kit by Abbott Ireland Diagnostics Division
Product group In-vitro diagnostics -
immunological products
|
| 28.05.2025 |
Urgent Field Safety Notice for Fujifilm Synapse PACS by FUJIFILM Medical System U.S.A., Inc.
Product group Radiological technology -
auxiliary equipment and supplies for radiology / nuclear medicine
|
| 28.05.2025 |
Urgent Field Safety Notice for Copeland Fetal Scalp Electrode by Rocket Medical plc
Product group Medical electronics / Electromedical devices -
electrodiagnostics
|
| 28.05.2025 |
Urgent Field Safety Notice for INSTINCT PLUS ENDOSCOPIC CLIPPING DEVICE by Wilson-Cook Medical, Inc
Product group Medical instruments for use in humans -
general instruments
|
| 28.05.2025 |
Urgent Field Safety Notice for LifePearl microspheres by MicroVention Europe
Product group Non-active implants -
special implants
|
| 27.05.2025 |
Urgent Field Safety Notice for UROSKOP OMNIA and UROSKOP OMNIA MAX by Siemens Healthcare GmbH, X-Ray Products (XP)
Product group Radiological technology -
radiological equipment for urological diagnostics
|
| 26.05.2025 |
Urgent Field Safety Notice for ORBIS Medication by DH Healthcare GmbH
Product group Medical data processing (software) -
others
|
| 26.05.2025 |
Urgent Field Safety Notice for Valve manifold set by PMH-Produtos Médico Hospitalares, S.A.
Product group Injections / Infusions / Transfusions / Dialysis -
infusion kits
|
| 26.05.2025 |
Urgent Field Safety Notice for ORBIS Medication by DH Healthcare GmbH
Product group Medical data processing (software) -
others
|