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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05.03.2010 |
Additional corrective action for Histopaque 1077-1 and Histopaque 1119-1, Sigma-Aldrich
Product group In-vitro diagnostics
|
15.05.2012 |
Additional Field Safety Notice for ARCHITECT Active-B12, Abbott
Product group In-vitro diagnostics -
equipment / products for clinical chemistry
|
29.01.2015 |
Additional important Information about CEM™ Nosecones for use with CUSA® Excel/Excel+ Ultrasonic Aspirator, Integra LifeSciences (Ireland) Limited
Product group Ultrasonics -
ultrasonic therapeutic equipment
|
21.07.2014 |
Additional Information / Recall for the Raucodrape NaCl Bowl Drape, Laboratoires Lohmann & Rauscher
Product group Surgical equipment/ Anaesthesia -
surgical equipment
|
09.08.2012 |
Additional Information about the Lot Recall of Creatinine (CREA) Flex reagent cartridges, Siemens
Product group In-vitro diagnostics -
equipment / products for clinical chemistry
|
08.10.2014 |
Additional Information concerning Harmonie™, Dynamis™ und Gerialit™ Hospital beds, Hill-Rom
Product group General equipment for medical treatment -
furnishings
|
25.07.2013 |
Additional Information concerning the corrective action for AMH Gen II Elisa, Beckman Coulter
Product group In-vitro diagnostics -
immunological products
|
03.07.2012 |
Additional Information concerning the Recall for Roticulator Single Use Stapler, Covidien
Product group Medical instruments for use in humans -
general instruments
|
23.05.2014 |
Additional Information for IMMULITE®/IMMULITE® 1000 and IMMULITE® 2000/IMMULITE® 2000 XPi Androstenedione assays, Siemens
Product group In-vitro diagnostics -
immunological products
|
31.03.2010 |
Additional Information for INFusor and FOLFusor pumps, Baxter
Product group Injections / Infusions / Transfusions / Dialysis
|