Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
3.599 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
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Siemens Healthcare Diagnostics AIMC 22-03 - Atellica® Solution and ADVIA Centaur® Systems
Siemens Healthcare Diagnostics Inc. has confirmed customer observations of falsely elevated results when using plasma specimens ...
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Getinge Disinfection CAPA 555530 - Getinge 9100-series - Washer Disinfector
Getinge has discovered that verification of installation is not always documented or the documentation is incomplete and does not ...
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Siemens Healthcare Diagnostics POC 22-002 - Atellica® UAS 800 Urine Sediment Analyzer & Atellica® 1500 Automated Urinalysis System
Siemens Healthcare Diagnostics has confirmed that the door gas spring which holds the analyzer door open is failing before its ...
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Abbott Molecular FA-AM-MAR2022-269 - Alinity m HBV AMP Kit
Abbott has received reports of falsely elevated results when using the Alinity m HBV AMP Kit. Data analysis has determined that ...
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SENTINEL FSCA 01/2022 - CALiaGOLD Control Set
An accuracy issue using Sentinel CALiaGold® Control Set REF 1151200 has been encountered, when testing the control material, ...
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GE Medical Systems, Revolution CT
De geaccumuleerde dosis wordt verkeerd weergegeven tijdens een interventioneel onderzoek met de SmartStep-optie.
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ARCHEON, FSN-FSCA-2022-N°01, EOlife®, EOlife® Premium Pack
The conversion to SLM does not consider the expansion of the gas at room temperature and the atmospheric pressure to adjust the ...
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Roche Diabetes Care SB_RDC_2022_02 - RocheDiabetes Care Platform HCP_M
Roche Diabetes Care became aware of a potential patient data mismatch when using the browser’s “back” button to navigate between ...
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Abbott FA-Q122-CRM-1 - Merlin™ and Merlin™2 Patient Care System (PCS)
Indien een gebruiker de knop “Hold to Test” indrukt en besluit te stoppen met testen door de knop los te laten voordat de eerste ...
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Merit Medical Systems Inc., FSN-1721504-03/01/22-002R, Access-9™ and AccessPLUS™ Hemostasis Valves
Merit Medical Systems, Inc. roept vrijwillig de Access-9™- en AccessPLUS™-hemostasekleppen terug vanwege een defect als gevolg ...