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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23.06.2006 |
Warning for OMNEX Surgical Sealant from the company Ethicon
Product group Non-active implants
|
22.08.2006 |
Warning for Calstrux from Stryker
Product group Non-active implants
|
20.07.2006 |
Warning against condom special offers in the Internet
Product group Contraception
|
14.10.2014 |
Waldemar Link GmbH & Co. KG: Recall for the Endo-Model® SL® – Connection Component, small
Product group Non-active implants -
bone surgery
|
07.07.2005 |
Vygon recalls the Catheter Reservoir PR06x and PR07x
Product group Non-active implants
|
08.10.2015 |
Voluntary Recall of Specific Serial Numbers of ConforMIS Knee Replacement Systems, ConforMIS
Product group Medical instruments for use in humans -
bone surgery
|
27.11.2013 |
Voluntary Recall of Anaconda™-ONE-LOK Bifurcate Body and Anaconda™ Bifurcate Body, VASCUTEK Ltd.
Product group Non-active implants -
special implants
|
16.02.2006 |
VOCO recalls Rebilda composits
Product group Dental products
|
20.02.2006 |
Visine Ophthalmics recalls the products Visine Tired Eyes Sensitive, Visine Tired Eyes and Visine Intensive
Product group ophthalmological technology
|
10.03.2006 |
Venous Line Clamp Occlusion Failure on hemodialysis instruments SYSTEM 1000, TINA, AURORA and ARENA from Baxter
Product group Injections / Infusions / Transfusions / Dialysis
|