Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
164 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
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Olympus Medical Systems Corporation, FSN-QIL 153-016, Olympus TJF-Q170V &TJF-Q190V & TJF-Q290 & MAJ-2315
The safety notice pertains to the referenced Olympus endoscope models and the disposable distal cover: DUODENOVIDEOSCOPE ...
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Olympus QIL 153-016 - DUODENOVIDEOSCOPE TJF-Q170_TJF-Q190V_TJF-Q290V and DISTAL COVER MAJ-2315
Olympus has identified an increase in the number of complaints from customers reporting that mucosal tissue was found within the ...
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Gambro Lundia AB, FSN-FA-2021-005, Prismaflex Control Unit
Healthcare Corporation is issuing a Device Correction to the user level for the Prismaflex Control Unit due.
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Medtronic, Inc., FSN-FA952, Strata II, Delta and Flow Control Valve
Het doel van deze brief is u te informeren over een mogelijke variatie in zichtbaarheid van radiopaque markeringen tijdens ...
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Baxter Healthcare SA, FSN-FA-2020-065, PRISMAX, V2 ROW
Baxter Healthcare Corporation is issuing a Device Correction for the PrisMax System due to inconsistent variability of the tubing ...
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Baxter Healthcare SA, FSN-FA-2020-064, PrisMax, V2, ROW
Baxter Healthcare is issuing a Safety Alert for the PrisMax System.
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Olympus Medical Systems Corporation, FSN-QIL 153-015, GASTROINTESTINAL VIDEOSCOPE / COLONOVIDEOSCOPE
URGENT FIELD SAFETY NOTICE QUARANTINE OF THE EZ1500 SERIES ENDOSCOPES.
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GAMBRO DASCO, FSN-FA-2020-068, Haemodialysis tubing set single-use
Baxter Healthcare Corporation has received customer reports of kinked access lines observed during treatment using cartridge sets ...
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Medtronic Inc., FSN-FA949, Intellis Clinician Programmer Application
Medtronic vaardigt vrijwillig een dringende veiligheidskennisgeving uit om te verzoeken dat u de Intellis™-softwaretoepassing ...
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Medtronic, Inc., FSN-FA948, ARESTM Antibiotic-Impregnated Catheter
Medtronic roept vrijwillig specifieke partijen ARES™ met antibiotica geïmpregneerde shuntkatheters terug.