Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
105 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
- Datum
- Relevantie
-
MatOrtho Limited, FSN-IE-2021-11-22-123, PIPR™
This FSN is to inform you that the indications and contraindications in the current instructions for use for these devices have ...
-
SYNTHES GMBH, FSN-2050712, Universal Chuck
Dit product wordt teruggeroepen vanwege een mogelijk probleem met het ontwerp van de bovenkap van de klauwkop. De bovenste kap ...
-
EUROS SAS, FSN-FSCA-2021-02, NEMOST - Growing Domino - Ø5.5mm
Following trend analysis in complaints related to NEMOST device, EUROS has decided to issue a voluntary safety notice to all ...
-
Biomet Microfixation LLC, FSN-ZFA 2021-00204, LACTOSORB TRAUMA PLATING SYSTEM
As a precautionary measure, Biomet Microfixation LLC is conducting a lot specific medical device Field Safety Corrective Action ...
-
DePuy Ireland FA 2044436 - GLOBAL UNITE STEM
Het betreffende product wordt verwijderd omdat DePuy (Ierland) heeft vastgesteld dat veel Global UNITE-stelen een ondermaatse ...
-
Acumed R21-006 - T15 Stick Fit Hexalobe Drivers
It has come to Acumed’s attention that two batches of T15 Stick Fit Hexalobe Drivers have features out of specification. The ...
-
SERF, FSN-2021-10, Reusable instruments SERF
Products delivered by SERF have been cleaned with a washer-disinfector, the automatic cleaning process mentioned in the ...
-
Medtronic Sofamor Danek USA, Inc., FSN-FA973, Break-off set screw
Medtronic is voluntarily recalling two lots of the Braive™ Break off Set Screw that are impacted by a thread profile defect due ...
-
MEDARTIS AG FSCA-2020-001 - MODUS and MODUS 2 Pliers
The previous information contained in the IFU was not specific enough for the following pliers: - M2-2016 2.0-2.5 Three-Point ...
-
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 ...