Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
3.593 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
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Maquet Cardiopulmonary GmbH, 812435, Rotaflow II drive flex.compact
In October 2022 Maquet Cardiopulmonary received a complaint on issues connected to the yellow locking mechanism unlocking on ...
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NVT GmbH, FSN-CAPA 23-10, ALLEGRA Transcatheter Heart Valve
NVT has been informed that there has been a mix-up between an ALLEGRA THV 23 and an ALLEGRA THV 31.lf not identified prior to ...
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Inter-med, Inc., FSN-RMA 41793, Septodont Parcan N NaOCL 3% Solution
During an endodontic procedure involving the use of Parcan N 3% NaOCl for irrigation of the root canal, the patient experienced ...
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Olympus Medical Systems Corporation, FSN-QIL FY24-EMEA-10-FY24-OMSC-05, PowerSpiral Intestinal Videoscope PSF-1
Recall - Market removal of PowerSpiral PSF-1 and associated accessories DPST-1 and PSCU Olympus had become aware of a situation ...
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FSN-AX008/23/S (FSCA), AX009/23/S (FSN), Siemens Healthcare GmbH, ARTIS pheno/icono
Due to a hardware issue in the cable connectors of the system generator, a thermal overload in the cable connections may occur in ...
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FSN-FSCA 272, Aesculap AG, Laparoscopic access
We detected a non-conformity to the product specification of part number FF399R caused by a manufacturing deviation. The affected ...
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Olympus Winter and Ibe GmbH, FY24-EMEA-01, HF-resection electrode
OLYMPUS has initiated this FSCA after receiving complaints where the loop wire at the distal end of the HF resection electrode ...
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Ambu A/S, FSN-Ambu2023FA00001, Ambu® aView 2 Advance
Ambu heeft informatie ontvangen waarbij Ambu® aView™ 2 Advance op de grond is gevallen, waarna er kortsluiting optrad en het ...
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VYGON, FSN-23 0203, Kocher forceps in delivery sets
When Kocher forceps are used for clamping the umbilical cord, a permanent monitoring must be ensured to prevent them from ...
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QuidelOrtho Ortho Clinical Diagnostics Inc, CL2023-145, ORTHO VISION and VISION Max Analyzers for BioVue
There may be a risk to patient results if ORTHO Sera Anti-N was processed on an analyzer where it is not validated, and the ORTHO ...