Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
3.594 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
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Acutronic Medical Systems AG, FSCA-23-003, Acutronic Medical Systems AG TV1 Ventilator
The device life of 5 years has been reached and/or exceeded for the TV1 Ventilators. As Acutronic will no longer be supporting ...
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Medline International France SAS, FSCA-23/07 / FSCA-23-07, Magnetic Instrument Drape MDL1CE
Medline brengt deze terugroeping uit om klanten te informeren over de mogelijkheid van een zwakke verzegeling die de steriele ...
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Bard Peripheral Vascular, Inc., PI-23-4795, Bard Marquee Disposable Core Biopsy Instrument Kit
Op basis van feedback van klanten heeft BD vastgesteld dat de diameter van de coaxiale canule en de biopsienaald (snijcanule) in ...
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Premier Guard Zhongshan Limited, 3503, Quest Spectrum Drape for Open Surgery PG
Quest has initiated this FSCA removal action after receiving a complaint regarding the plastic cover glass of the drape that ...
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AB SCIEX Pte. Ltd., FSCA-2023-177083, 4500MD and Citrine LC-MS/MS Systems
In rare occasions, the combination of a leak of a highly flammable solvent at the ion source pro be, and an electrical discharge ...
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Hamilton Medical AG, FSCA 2023-07-03, HAMILTON-C1, HAMILTON-T1, HAMILTON-MR1
A degrading capacitor on the control board might leak electrolyte onto the control board, causing a short circuit on the board ...
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Beckman Coulter, Inc., FA 23026, Access Folate (Reagent Pack)
Beckman Coulter heeft vastgesteld dat de reagenspipetten voor de DxI 9000 Access-immunoassay-analyser mogelijk niet volledig door ...
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PEROUSE MEDICAL, CAPA23-051, POLYFILM
A sealing problem on the packaging of the POLYFILM® has occurred. If the packaging of POLYFILM® has a defective sealing, it can ...
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Löwenstein Medical Innovation GmbH & Co. KG, FSCA2023011, elisa 300. elisa 500. elisa 600. elisa 800
Tijdens het monitoren van de markt zijn we ons bewust geworden van 3 gevallen waarin vertraagde herkenning van de patiënt kan ...
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Datascope Corp., 2249723-06.02.2023-014-C, Cardiosave Intra-Aortic Balloon Pumps
Datascope/Getinge identified that 182 of these complaints were directly related to the IABP and described failure mode.