Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
3.325 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
- Datum
- Relevantie
-
Biohit Oyj, 144-22, BIOHIT ColonView quick test
lf the specified kit lot has been used, a minor possibility for a false negative result still exists. In such a case there would ...
-
Aesculap AG, FSCA 266, Nasal snare single-use
Aesculap AG as a legal manufacturer has voluntarily decided to recall the affected products under point 1.2 as a precaution due ...
-
Biomet Orthopedic LLC, ZFA2022-00204, Oxford Fixed Lateral
Biomet Orthopedics LLC is conducting a lot specific medical device Field Safety Corrective Action (removal) for certain Oxford ...
-
Bolton Medical Inc, 2247858-12-06-2022-001R, RelayPro Thoracic Stent Graft System
The Efficia External Paddles are intended to be used with the Efficia DFM100 and HeartStart Intrepid Monitor/Defibrillators – by ...
-
Philips Goldway Shenzhen Industrial Inc., 2021-CC-EC-023-IR, Efficia External Paddles
The Efficia External Paddles are intended to be used with the Efficia DFM100 and HeartStart Intrepid Monitor/Defibrillators – by ...
-
Philips Goldway Shenzhen Industrial Inc., 2022-CC-EC-010-IR, Efficia Pads Adapter Cable
Efficia DFM100 and HeartStart Intrepid Monitor/Defibrillators are at risk of failed ECG monitoring, defibrillation, synchronized ...
-
INTRASENSE, FSN-2022-01 (Azure Ref: 26966), Myrian
By default, Myrian® hides series of types scout, dose report and other documents to make the workspace clearer and only display ...
-
Safe Orthopaedics, FSN-22-03, CEMENT PUSHER KIT
Safe Orthopedics has detected an anomaly concerning the instructions for use of the Cement Pushers and Kit Needle kits. The ...
-
Teleflex Malaysia Sdn Bdh Malaysia, FSN-EIF-000523, RUSCHELIT® Super Safety Clear Tracheal Tube, oral/nasal, Murphy - and others
This voluntary FSCA for the above-listed products has been initiated due to reports of pilot balloon non-inflation or cuff ...
-
Osypka AG, FSCA_002_NCR_155_2022, Cardiac valvuloplasty catheter
Based on customer feedback, we have determined that a mix-up occurred during the labelling process for these products.