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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10.03.2006 |
Varian Medical Systems recalls Tongue and Soft Tissue Kits
Product group Radiotherapy / Radiation protection
|
21.11.2005 |
Varian informs about the effects of the VARiS Vision plan revision mechanism on total absolute dose distributions in Eclipse
Product group Radiotherapy / Radiation protection
|
03.06.2005 |
Varian ecalls the Flexible Implant tube, blind end
Product group Radiotherapy / Radiation protection
|
13.10.2005 |
User Information for the Lifepak 500 AED from Medtronic
Product group Medical electronics / Electromedical devices
|
17.06.2021 |
URGENT: FIELD SAFETY NOTICE Philips Respironics Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent, BiPAP V30, and BiPAP A30/A40 Series Device Models
Product group Surgical equipment/ Anaesthesia -
anaesthesia and medical gas supply
|
17.06.2021 |
URGENT: FIELD SAFETY NOTICE Philips Respironics CPAP and Bi-Level PAP Devices
Product group Surgical equipment/ Anaesthesia -
anaesthesia and medical gas supply
|
13.10.2015 |
URGENT: FIELD SAFETY NOTICE LifeCycle for Prenatal
Screening software Version v4.0 Rev4k, PerkinElmer
Product group In-vitro diagnostics -
equipment / products for clinical chemistry
|
12.12.2014 |
Urgent Safey Notice for the MetaVision® Suite, Clinical Information System version 5.4x, iMDsoft Ltd.
Product group Medical data processing (software) -
others
|
15.01.2015 |
Urgent Safety Notices for the Lactate membrane units, when used with ABL700 and ABL800 Series Analyzers, Radiometer
Product group In-vitro diagnostics -
equipment / products for clinical chemistry
|
07.07.2015 |
Urgent Safety Notice/Update for the Expel™ APD and APDL Drainage Catheters, Boston Scientific
Product group Injections / Infusions / Transfusions / Dialysis -
drainages and suction systems
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