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: |
|---|---|
| 13.12.2004 |
Exchange of all telescopic drives by chest x-ray Thoravision from Philips
Product group Radiological technology
|
| 13.12.2004 |
Aesculap recalls the products Orthopilot THA Reamer Shafts 40-48 HARR
Product group Medical instruments for use in humans
|
| 13.12.2004 |
Product safety advisory of the Signal Acquisition Module model 8300
Product group Medical electronics / Electromedical devices
|
| 15.12.2004 |
Communication problems with accelerator software Desktop Pro from Elekta
Product group Radiotherapy / Radiation protection
|
| 15.12.2004 |
Possibility of mismatching VAC and AIR sockets of Dräger AIR Dual PLUG Connector
Product group Surgical equipment/ Anaesthesia
|
| 15.12.2004 |
Corrective action of Olympus System Reagent Cholesterol and HDL Cholesterol, Olympus
Product group In-vitro diagnostics
|
| 15.12.2004 |
DPC Biermann recalls Immulite Insulin
Product group In-vitro diagnostics
|
| 15.12.2004 |
Corrective action for Thromborel S, Dade Behring
Product group In-vitro diagnostics
|
| 16.12.2004 |
Recall of several spinal and epidural anesthesia kits by Smiths Medical
Product group Injections / Infusions / Transfusions / Dialysis
|
| 16.12.2004 |
Dade Behring recalls the D-Dimer PLUS Testkits
Product group In-vitro diagnostics
|