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: |
---|---|
14.06.2024 |
Urgent Field Safety Notice for IH-1000 Analyzer by Bio-Rad Laboratories, DiaMed GmbH
Product group In-vitro diagnostics -
haematological, histological and cytological products
|
14.06.2024 |
Urgent Field Safety Notice for Bivona Neonatal/Pediatric and Adult Tracheostomy Tube by Smiths Medical ASD, lnc.
Product group Surgical equipment/ Anaesthesia -
anaesthesia and medical gas supply
|
14.06.2024 |
Urgent Field Safety Notice for DxI 9000 Access Immunoassay Analyzer by Beckman Coulter Inc.
Product group In-vitro diagnostics -
equipment / products for clinical chemistry
|
14.06.2024 |
Urgent Field Safety Notice for DxI 9000 Access Immunoassay Analyzer by Beckman Coulter Inc.
Product group In-vitro diagnostics -
equipment / products for clinical chemistry
|
14.06.2024 |
Urgent Field Safety Notice for Ascenda Intrathecal Catheter by Medtronic Inc
Product group Active implantable medical devices -
drug pumps
|
14.06.2024 |
Urgent Field Safety Notice for Afinion 2 by Abbott Diagnostics Technologies AS
Product group In-vitro diagnostics -
haematological, histological and cytological products
|
14.06.2024 |
Urgent Field Safety Notice for Hintermann Series H3 Total Ankle Replacement System by DT MedTech LLC
Product group Non-active implants -
bone surgery
|
13.06.2024 |
Urgent Field Safety Notice for NexGen CR-Flex porous or NexGen CR-Flex Fiber Metal Mesh Femur by Zimmer Inc.
Product group Non-active implants -
bone surgery
|
13.06.2024 |
Urgent Field Safety Notice for Connecting Tubes by Extrudan S.. z o.o Zakrzewo
Product group Injections / Infusions / Transfusions / Dialysis -
drainages and suction systems
|
13.06.2024 |
Urgent Field Safety Notice for RAL Diff-Quik Fixative solution by RAL DIAGNOSTICS
Product group In-vitro diagnostics -
haematological, histological and cytological products
|