Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
466 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
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Smith & Nephew R-2020-03 - Footprint Ultra PK Suture Anchor
Met deze brief willen wij u informeren dat Smith & Nephew, Inc. vrijwillig specifieke partijen van de Footprint Ultra PK Suture ...
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Promedon S.A #455 - CAPA N°; MDSS ref. MDD20.022 - VANTRIS VUR Treatment
Obstruction of the UVJ is a known but rare complication of any endoscopic treatment using bulking agents for the treatment of ...
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Medtronic FA906 - Pipeline Flex Embolization Device
Medtronic has identified the potential for device fracture at the distal section during use due to a weakened bond in a subset of ...
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Asclepion Laser Technologies GmbH FSA 2020-001 - MultiPulse HoPLUS
In a previously unique case under special conditions, it was found that the laser continued to laser approximately 50 seconds ...
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Neovasc Inc. FCA 19-001-C - Neovasc Reducer
Neovasc has discovered an error in the expiration date of the Reducer System Lot No. 190131-01. Since the Reducer Kit expiration ...
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Cook Endoscopy, Wilson-Cook Medical Inc. 2020FA0002 - Hemospray Endoscopic Hemostat
Cook Medical has received complaints regarding Hemospray Endoscopic Hemostat devices for the handle and/or activation knob ...
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Zimmer Biomet ZFA 2019-00322 - Calcar Trimmer Shaft
Biomet Orthopedics is conducting a medical device Field Safety Corrective Action (removal) for certain lots of the Calcar Trimmer ...
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Galil Medical SM091-2019 - Visual-ICE Cryoablation System
The desiccant tubes’ robustness and ability to remove moisture from the gas system may have been compromised. This additional ...
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Teleflex EIF-000392 - Pilling CLEAR ADVANTAGE
Teleflex voert een terugroepactie uit voor de bovenstaande productcodes en partijen zoals vermeld in Appendix 2. Het is mogelijk ...
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Stryker RA2020-2276634 - Telescopische rookafzuigpennen
Haarscheurtjes in een component kunnen elektrische stroom naar de buitenkant van de telescopische rookevacuatiepen geleiden.