Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
467 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
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Boston Scientific Corporation, FSN-92926415-FA, ORISE™ Gel Submucosal Lifting Agent
Boston Scientific heeft onlangs ontdekt dat er bijwerkingen optraden die werden gekoppeld aan een reactie op vreemde voorwerpen ...
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Ethicon 20-019 - 8-0 Blue Twisted Silk Suture
Ethicon informeert haar klanten over bepaalde productcodes van maat 8-0 blauwe gedraaide zijden hechtdraad.
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Leica Microsystems (Schweiz) AG, FSN-CAPA-HER-MD-21-002, Leica M220 F12
The identified defect is a mechanical part failure with the screw that connects the optics carrier to the free end of the swing ...
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Field Safety Notice: CONMED Corporation, Hyfrecator® 2000 Electrosurgical Units
From December 2, 2015 to January 3, 2017, the Accessory Packages in the Hyfrecator® 2000 ESU cartons were packaged in error by ...
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Field Safety Notice: Ethicon, Vicyrl Rapide 2-0 and 4-0 Suture Damage
Ethicon has initiated a medical device recall (removal) of certain lots of VICRYL RAPIDETM (Polyglactin 910) Suture. We have ...
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Field Safety Notice: Smith & Nephew - OSTEOTOME Blades
Door middel van deze brief delen wij u mee dat Smith & Nephew, Inc een productgroep OSTEOTOME BLADES vrijwillig terugroept ...
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Aesculap AG, FSCA 271, Tunneling instrument 600MM
In some cases, the sealing of the sterile secondary packaging was not carried out in accordance with the process for the products ...
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Johnson & Johnson International, Vicryl™ Plus Suture - 2207555, Coated VICRYL™ PLUS Antibacterial suture
Ethicon has initiated a voluntary medical device recall (removal) of one (1) lot of Coated VICRYL™ Plus Antibacterial ...
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Intuitive Surgical, ISIFA2022-05-C, Large / Medium-Large / Small Clip Applier
This Field Safety Notice is to notify you of the potential for unexpected motion while using the da Vinci S/Si and X/Xi EndoWrist ...
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Advanced Medical Solutions Ltd, FSN-01-31-2022-001-FSCA, LiquiBandFIX8® Open Hernia Mesh Fixation Device
AMS has become aware of a mechanical device defect in the Product during an internal testing of device. The defect causes ...