Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
467 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
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Zimmer Dental RN15-003 NL - Trabecular Metal Dental Implant
Through investigation, Zimmer Dental determined that information specific to the 3.7mmD and 4.1mmD Trabecular Metal implants was ...
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Coloplast FRALL-2015-1207 - ACA1xx & ACA2xx - VORTEK - Single Loop Ureteral Stent
De vervanging van de Vortek® Ureterale stents met enkele lus wordt niet beschreven in de huidige gebruiksaanwijzing (Instruction ...
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Bayer SA-15-RAD-12 & SA-15-RAD-14 - MEDRAD IntegoTM PET Source Administration Sets
Wij hebben geconstateerd dat bepaalde brontoedieningssets (SAS) die met het Medrad ® Intego PET-infusiesysteem worden gebruikt, ...
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Elekta FCA-EIAB-0003 - Leksell GammaPlan
Volumes representing planned dose from a previous treatment (sometimes referred to as “blue lines”) may be misplaced in the ...
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Johnson& Johnson R2015123 - Insertion Handle for PFN
Synthes GmbH is initiating a medical device recall of the below specified lots of Versions 1, 3.1 & 3.2 of the PFN/PFNA ...
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Johnson & Johnson thermachoice 111 Catheter Voluntary Recall - Gynecare thermachoice lll catheter
Ethicon, Inc. ("ETHICON") has initiated a voluntary recall of the GYNECARE THERMACHOICE™ III Thermal Balloon Ablation Silicone ...
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Medtronic EGIA Handles 11/15 - Endo GIA Ultra Universal Stapler 12mm
The purpose of this letter is to advise you that Medtronic is recalling specific item codes and production lots of Covidien Endo ...