Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
3.586 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
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Biocartis BC-013089 - Idylla™ EGFR Mutation Test
The Idylla™ EGFR Mutation Test Instructions for Use (IFU) has been updated based on customer feedback and a request received from ...
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Dräger PR93593 - Oxylog VE300
Within the framework of our continuous market surveillance activities, a case has come to our attention in which the Oxylog VE300 ...
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Baxter FA-2020-006 - Prismaflex Control Unit
Baxter is communicating important safety information regarding the use of connectors with the Prismaflex system. The use of ...
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BioMerieux Inc FSCA 4654 - VITEK® 2 AST-N371 TEST KIT 20 CARDS
A potential issue was identified relating to the top seal of card pouches for the VITEK® 2 test card lot AST-N371 0210932204. ...
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Zimmer Biomet ZFA 2019-00433 - Innex Anchorage Stems
As a precautionary measure Zimmer GmbH is conducting a medical device Field Safety Corrective Action (Removal) for specific lots ...
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Neovasc Inc. FCA 19-001-C - Neovasc Reducer
Neovasc has discovered an error in the expiration date of the Reducer System Lot No. 190131-01. Since the Reducer Kit expiration ...
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Baxter FA-2020-003 - Revaclear 500
Baxter Healthcare Corporation is issuing a voluntary product recall for one lot of Revaclear 500 Dialyzers due to reports of ...
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Medtronic_Bellco FA904 - Bellco MICROPLAS Plasmafilters
We voeren deze vrijwillige recall uit omdat de MICROPLAS-plasmafilters verkeerd gebruikt kunnen worden. Medtronic (Bellco) ...
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Innotere GmbH 20200214 - INNOTERE Paste-CPC
We hereby inform you about an field safety notice on the dosage of Paste-CPC. Due to new scientific findings on the excipient ...
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Siemens POC 20-001 - CLINITEK Status+ Analyzer and CLINITEK Status Connect Platform
Siemens Healthcare Diagnostics has confirmed that the CLINITEK Status® Connect System could transmit incorrect results to the ...