Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
3.586 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
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Itémedical BV FSCA 03126 - MediScore MIM
With [Automatically enter a specific dose] button configuration within MetaVision 5.46 MediScore MIM receives wrong date/time ...
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Gambro Lundia, FA-2019-023, Prismaflex System
Er is vastgesteld dat de calcium-spuitpomp inactief kan worden zonder dat het alarm afgaat wanneer de spuit vervangen is.
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Roche Diagnostics, IO-0000163, Elecsys Syphilis (200 test/kit),
Erroneous Values used for Interference of IgM and IgG
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bioMerieux Inc, FSCA 4360, Chocolat PolyViteX (PVX)
We hebben klachten ontvangen van klanten over een afwijkende groei (beperkt of afwezig) voor de volgende stammen:...
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Randox Laboratories, REC398, HUMAN ASSAYED MULTI-SERA Level 2
Randox has identified a labelling error in the value sheet for Human Assayed Controls Level 2 lots 1306UN, 1308UN and 1309UN.
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Philips, FSCA 79500509-519A-IR, Philips-EPIQ and Affiniti Ultrasound system
Philips heeft recentelijk een softwareprobleem ontdekt met de functie Edit (Wijzigen) op de pagina Patient Data Entry (PDE; ...
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Roche Diagnostics, CN-451459, AssayTip/AssayCup
We wish to advise that we have identified defective assay cups from lots 19817113 and 19818113
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Roche Diagnostics, CN-431825, IGA-2 (Tina-quant IgA Gen.2)
Internal investigations of the affected c packs revealed contamination of R1 with R3 (containing antibody).
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Biomet, ZFA 2019-00113, Oxford Knee Anatomic Meniscal Bearing
A complaint investigation revealed that a left handed bearing had been supplied within the package labeled for a right handed ...
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Siemens, ACHC 19-02, Atellica and ADVIA Creatine Kinase (CK_L) Reagent
The purpose of this communication is to inform you of an issue with the products listed in Table 1 above and provide instructions ...