Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
46 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
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- Relevantie
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Align Technology, CMD-67847, Invisalign System
As a result of the software release on June 1, 2019, in some instances, customers were able to modify and re-approve a number of ...
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Villa Sistemi Medicali S.p.A., M18022, Apollo - DRF - EZ - EZ DRF- Clinodigit EVO, JUnoDFR
Therefore, the Ifu and the Service Manual need to me amended...
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Siemens CC 19-07 - ADVIA Centaur Folate
Siemens Healthcare Diagnostics has confirmed the potential for the ADVIA Centaur Homocysteine assay (100 Test Kit SMN 10310374; ...
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Skulle Implants FSN0719 - GLACE Screws 6 mm
Skulle Implants Corporation is conducting a medical device Field Safety Corrective Action for the GLACETM CMF 6 mm screws due to ...
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MICRO-MEGA SA, NC_AQC_201901_021, X-Cid2
Als de gebruiker de externe restanten niet verwijdert voor het toestel in de X-Cid2 gaat, is het mogelijk dat de buitenkant van ...
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Implant Direct Sybron Manufacturing, HHE-8037P10rev01, Legacy™P Implant
Er is een verkeerde maat implantaat verpakt.
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Nobel Biocare, PFA1906, drills etc
Due to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the ...
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Biomet, ZFA 2019-00009, LactoSorb RapidFlap
Zimmer Biomet CMF and Thoracic, LLC (“Zimmer Biomet”) is conducting a medical device removal for certain lot numbers of the ...
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XO CARE A/S MLHN-AEWDNP-FSCA - Dental units XO 4 and XO FLEX
The suction hoses for the XO Units, containing magnets, have the potential to negatively impact implanted pacemakers and ...
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Zimmer, RHD2.5 Hex Driver, 2023141-10-04-2017-002-R
Zimmer Biomet voert een terugroepactie van medische producten uit voor de 2,5 mm GemLock Hex Driver, RHD2.5.