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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28.06.2024 |
Urgent Field Safety Notice for Pflegebett Ecofit/Ecofit S by tecfor care GmbH
Product group General equipment for medical treatment -
furnishings
|
28.06.2024 |
Urgent Field Safety Notice for Pflegebett Ecofit/Ecofit S by tecfor care GmbH
Product group General equipment for medical treatment -
furnishings
|
28.06.2024 |
Urgent Field Safety Notice for SYNCHRO Guidewires by Stryker Neurovascular-Caliifornia
Product group Injections / Infusions / Transfusions / Dialysis -
catheters
|
28.06.2024 |
Urgent Field Safety Notice for NADAL Troponin I Test by nal von minden GmbH
Product group In-vitro diagnostics -
immunological products
|
28.06.2024 |
Urgent Field Safety Notice for Luminos Agile/dRF/Lotus Max, Multitom Rax by Siemens Healthcare GmbH, X-Ray Products (XP)
Product group Radiological technology -
stationary radiological equipment
|
28.06.2024 |
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 IMMULITE/IMMULITE 1000 TNF -alfa by Siemens Healthcare Diagnostics Products Ltd.
Product group In-vitro diagnostics -
immunological products
|
27.06.2024 |
Urgent Field Safety Notice for DISCOVERY HUMERAL STEMS by LIMACORPORATE S.P.A.
Product group Non-active implants -
bone surgery
|
27.06.2024 |
Urgent Field Safety Notice for ILED 7 CEILING SINGLE ILED 7 MOBILE ILED 7 PENDANT by Baxter Medical Systems GmbH + Co. KG
Product group Surgical equipment/ Anaesthesia -
surgical equipment
|
27.06.2024 |
Urgent Field Safety Notice for Transystem / Specimen collection device 900-0370 by Copan Italia S.p.A.
Product group General equipment for medical treatment -
auxiliary equipment
|