Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
3.325 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
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Siemens Healthcare, UI XP051/22/S, AXIOM Iconos R100; R200 C20+C90; AXIOM Luminos TF
Potential risk of foot rest detaching from the patient table
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Siemens Healthcare, AX017/22/S (FSCA), AX018/22/S (FSN), ARTIS pheno
Three potential software issues on all ARTIS pheno systems with software version VE10B
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Leica Biosystems Newcastle, IR 66/22, NovocastraTM Muscle Specific Actin
Leica Biosystems Newcastle recently became aware the IFU of affected device mentioned above incorrectly states a suggested ...
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Medtronic Inc., FA1292, Vanta LT Clinician Programmer Application
Met deze brief informeren wij u over een mogelijk communicatieprobleem als gevolg van een softwareafwijking met de Vanta™ ...
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HeartWare Inc., FA1293, HeartWare™ Ventricular Assist Device (HVAD™) System Hardened Driveline Cover.
Medtronic maakt u attent op belangrijke veiligheidsinformatie over de kap van de aandrijflijncontroller van het HVAD™- systeem. ...
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Clinical Innovations LLC, FSCA 2022-CC-HPM-061, Fetal Measurements
Philips has become aware of a potential safety issue with the Fetal Spiral Electrode (FSE) based on complaints related to the ...
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Nucletron B.V., FCA-NU-0008, Oncentra brachy
Er kan een reconstructiefout optreden bij gebruik van de functie Catheter Bending (Katheter buigen) in Applicator Modeling ...
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Randox Laboratories Ltd., REC629, Randox Specific Protein Control Levels 1-3
Rheumatoid Factor (RF) is a protein whose levels are increased in patients with Rheumatoid Arthritis. Delay in reporting results ...
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Heater Cooler B.V., 2072095, HCTronic
We would like to inform you about a software bug we found because of feedback we received on 21 November 2022.
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Abbott Molecular, FA-AM-NOV2022-283, Alinity m Resp-4-Plex AMP Kit
Abbott has received reports of an increase in reactive negative controls and false positive results, with certain lots of Alinity ...