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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05.01.2005 |
Recall of Ortho Clinical Diagnostics for Vitros Immunodiagnostic Products
Product group In-vitro diagnostics
|
06.01.2005 |
Wright Medical Technologies recalls the Conserve Plus acetabular components
Product group Non-active implants
|
07.01.2005 |
Recall of Biotrin for Parvovirus B19 Immunofluorescent Assay
Product group In-vitro diagnostics
|
10.01.2005 |
Aesculap recalls Columbus CR Femoral Components
Product group Non-active implants
|
10.01.2005 |
Weight restrictions for Bicontact SD and Bicontact SD-Revision implants from Aesculap
Product group Non-active implants
|
10.01.2005 |
Accutrend Glucose test strips in falsified packages, Roche
Product group In-vitro diagnostics
|
10.01.2005 |
Corrective action of Roche for Gluc/(Lac/Urea) cassettes
Product group In-vitro diagnostics
|
13.01.2005 |
Software failure of CIC Pro Central Stations from GE Medical Systems
Product group Medical electronics / Electromedical devices
|
13.01.2005 |
Corrective action of Beckman Coulter for Coulter LH 750 Hematology Analyzers
Product group In-vitro diagnostics
|
14.01.2005 |
Boston Scientific recalls detachable coils GDC
Product group Non-active implants
|