Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
3.599 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
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Siemens, AX077/21/S; AX078/21/S & AX081/21/S, Sensis etc
Under certain sporadic circumstances it can happen that on a Sensis Vibe Hemo system with VD12A software the CO (Cardiac Output) ...
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Philips, 2021-IGT-BST-020, Philips Allura Xper and Azurion systems
Verbindingsproblemen met de draadloze voetschakelaar veroorzaken onderbreking van fluoroscopie en opname.
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VitreQ, PRE-20210004, VitreQ
VitreQ B.V. is issuing this Field Safety Notice to make you aware of a mislabeling of three vitreoretinal 25G Disposable Micro ...
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Avanos Medical, FCA-2021-006, Multi-Access Port Closed Suction System for Adults
Avanos has detected through a regular review of the Label Room Spreadsheet that on the Label Room Spreadsheet (a password ...
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Eco-Med Pharmaceutical, EcoGel 200
We are instructing you to immediately stop using and discard all coupling gels manufactured by Eco-Med Pharmaceutical Inc. due to ...
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Medtronic, FA1183, Recharger Kit
Medtronic heeft door middel van klachtenevaluatie vastgesteld dat zich bij de Medtronic-oplader WR9200, die worden geleverd bij ...
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BIOTRONIK AG, 200000470, Passeo-35 Xeo
During an in-house inspection, Biotronik discovered that a few sterilization pouches of the Passeo-35 Xeo and Dynetic-35 were ...
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BIOTRONIK, 200000470, Dynetic-35
During an in-house inspection, Biotronik discovered that a few sterilization pouches of the Passeo-35 Xeo and Dynetic-35 were ...
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Baylis Medical Comany, Recall 2111-01, NRG transseptale naald
Baylis Medical Company Inc. roept vrijwillig 5 eenheden van de NRG transseptale naald terug wegens het ontbreken van een ...
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Siemens, VSW 22-01, Dimension Vista Systems
Incorrect Default Hemolysis, Icterus or Lipemia (HIL) Index for Five Dimension Vista Assays