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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05.07.2024 |
Urgent Field Safety Notice for Puritan Bennett 500 Series Ventilator by Covidien llc
Product group Surgical equipment/ Anaesthesia -
anaesthesia and medical gas supply
|
05.07.2024 |
Urgent Field Safety Notice for ORBIS Medication by DH Healthcare GmbH
Product group Medical data processing (software) -
others
|
04.07.2024 |
Urgent Field Safety Notice for Centricity High Acuity (CHA) C.C and Anesthesia by GE Healthcare Finland Oy
Product group Medical electronics / Electromedical devices -
electrodiagnostics
|
03.07.2024 |
Urgent Field Safety Notice for IntelliVue X3 by Philips Medizin Systeme Boblingen GmbH
Product group Medical electronics / Electromedical devices -
electrodiagnostics
|
02.07.2024 |
Urgent Field Safety Notice for VENUS by HumanTech Germany GmbH
Product group Non-active implants -
bone surgery
|
02.07.2024 |
Urgent Field Safety Notice for Alcotest 7000 med by Dräger Safety AG & Co. KGaA
Product group Medical electronics / Electromedical devices -
functional diagnostics by way of gas exchange and exercise
|
02.07.2024 |
Urgent Field Safety Notice for Defigard Touch 7 by Schiller Medical SAS
Product group Medical electronics / Electromedical devices -
electrotherapy
|
01.07.2024 |
Urgent Field Safety Notice for Capio SLIM Suture Capturing Device by Boston Scientific Corporation Marlborough
Product group Medical instruments for use in humans -
general instruments
|
01.07.2024 |
Urgent Field Safety Notice for STARKLING / Starkling Anesthesia by Starkling e.K.
Product group Optics / Precision engineering -
medical microscopes (does not incude laboratory microscopes)
|
28.06.2024 |
Urgent Field Safety Notice for Pflegebett Ecofit/Ecofit S by tecfor care GmbH
Product group General equipment for medical treatment -
furnishings
|