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: |
|---|---|
| 19.09.2025 |
Urgent Field Safety Notice for ERYTRA by Diagnostic Grifols SA
Product group In-vitro diagnostics -
haematological, histological and cytological products
|
| 18.09.2025 |
Urgent Field Safety Notice for CellMek SPS by Beckman Coulter, Inc.
Product group In-vitro diagnostics -
equipment / products for clinical chemistry
|
| 18.09.2025 |
Urgent Field Safety Notice for MADSEN AccuScreen TEAOE/DPOAE/ABR Probe by PATH MEDICAL GmbH
Product group Medical electronics / Electromedical devices -
ENT equipment
|
| 18.09.2025 |
Urgent Field Safety Notice for AIRVO2 Humidifier / myAIRVO2 Humidifier by Fisher & Paykel Healthcare Ltd
Product group Surgical equipment/ Anaesthesia -
anaesthesia and medical gas supply
|
| 18.09.2025 |
Urgent Field Safety Notice for TactiFlex Force Sensing Ablation Catheter, S. by Abbott Plymouth, Product Performance Group
Product group Injections / Infusions / Transfusions / Dialysis -
catheters
|
| 18.09.2025 |
Urgent Field Safety Notice for Inogen Rove 4 Portable Oxygen Concentrator by Inogen, Inc.
Product group Physical therapy -
equipment for oxygen therapy
|
| 18.09.2025 |
Urgent Field Safety Notice for Catalyft PL Expandable Interbody System by Medtronic Sofamor Danek Inc.
Product group Non-active implants -
bone surgery
|
| 18.09.2025 |
Urgent Field Safety Notice for BRONCHOVIDEOSCOPE and BRONCHOFIBERSCOPE, divers by Olympus Medical Systems Corp.
Product group Optics / Precision engineering -
endoscopes
|
| 17.09.2025 |
Urgent Field Safety Notice for MRI System by Siemens Healthcare GmbH - Diagnostic Imaging
Product group Electromedical fields -
equipment for MR tomography
|
| 16.09.2025 |
Urgent Field Safety Notice for Magnet Venting Path of 3 Tesla MRI System by Siemens Shenzhen Magnetic Resonance Ltd.
Product group Electromedical fields -
equipment for MR tomography
|