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.
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Date | Title: |
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04.11.2011 |
Additional Information for Medstream Implantable Drug Infusion Pump, Codman
Product group Active implantable medical devices
|
18.05.2010 |
Additional Information for NexGen Trabecular Metal Tibial Trays, Zimmer Inc.
Product group Non-active implants
|
05.02.2015 |
Additional Information for the AB SCIEX IVD-MS™ Analyzer device, AB SCIEX
Product group In-vitro diagnostics -
equipment / products for clinical chemistry
|
27.06.2014 |
Additional Information for the Altrus® Thermal Tissue Fusion Handpieces, ConMed
Product group Medical electronics / Electromedical devices -
electrotherapy
|
13.04.2015 |
Additional Information for the Bead Block (Embolic Bead) device, Biocompatibles UK Ltd.
Product group Non-active implants -
special implants
|
23.06.2015 |
Additional Information for the CombiSets® containing Medtronic Covidien Devon™ Light Glove, Paul Hartmann AG
Product group Surgical equipment/ Anaesthesia -
surgical equipment
|
22.04.2015 |
Additional Information for the pCO2 Membrane Box (D788) used with ABL700 and ABL800 Series Analyzers, Radiometer GmbH
Product group In-vitro diagnostics -
equipment / products for clinical chemistry
|
15.12.2011 |
Additional Information: Lot Recall of different dialysis tubing systems, Gambro
Product group Injections / Infusions / Transfusions / Dialysis
|
17.03.2014 |
Additional Instruction for Use for the Edi catheter, Maquet Critical Care AB
Product group Injections / Infusions / Transfusions / Dialysis -
probes
|
06.02.2012 |
Additional Lot-No. on recall of Lupine Loop Anker, DePuy
Product group Non-active implants -
bone surgery
|