Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
202 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
- Datum
- Relevantie
-
Synthes GmbH 1637139 - USS II Polyaxial
Synthes GmbH initieert een vrijwillige terugroepactie van “USS II Polyaxial 3D Heads”. Informatie over het product wordt in tabel ...
-
Stryker Joint Replacement, RA2024-3598242, Mako Total Knee
Stryker has discovered specific to the applications listed in Table 1 an increase in the Software Error #3 (SE3) error code when ...
-
Zimmer Biomet ZFA 2020-00331 - Vanguard 360 Revision System
As a precautionary measure Biomet Orthopedics LLC is conducting a medical device Field Safety Corrective Action (Removal) for a ...
-
AREX®, FSN-FSCA20200928, Mini external fixator - HK2
Modifications on the IFU and on the label of HK2.
-
TORNIER SAS, FSN-FA-WMG-2020-003, Inspyre™ Implant
Informatie met betrekking tot de bijwerking van de gebruiksaanwijzing voor de Inspyre™ Implant.
-
AREX®, FSN-FSCA20200724, LIGAMENTOTAXOR / LTX
Nadat een LIGAMENTOTAXOR na implantatie kapot is gegaan heeft de firma AREX® besloten voorschriften op te stellen voor de goede ...
-
Zimmer Biomet ZFA 2020-00012 - Comprehensive Reverse Shoulder System
Biomet Orthopedics is conducting a medical device field safety corrective action (removal) for onesingle lot of the Comprehensive ...
-
Biomet UK Ltd - ZFA 2019-00103 - Biolox Hip Option Taper Adapter
Biomet UK Ltd. is conducting a medical device Field Safety Corrective Action (removal) for specific lots of Biolox Hip Option ...
-
Biomet, ZFA 2019-00113, Oxford Knee Anatomic Meniscal Bearing
A complaint investigation revealed that a left handed bearing had been supplied within the package labeled for a right handed ...
-
Zimmer, ZFA2017-385, Vanguard
Product complaints indicate that the lots were comingled.