Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen

1. Medtronic FA1231- Percept™ PC Implantable Neurostimulator

   Het doel van deze brief is u mede te delen dat in zeldzame gevallen (0,044%) de Percept™ PC-implanteerbare neurostimulator (INS) ...

   Waarschuwing | 20-04-2022

2. Acandis GmbH FSCA 22-001 - DERIVO® 2 Embolisation Device

   We have received an increasing number of complaints from customers who have reported difficulty in delivery of devices through ...

   Waarschuwing | 26-01-2022

3. Technomed Europe CAPA 21-009_NCR 21-081 - Disposable Subdermal Needle Electrode, corkscrew

   Technomed is issuing a Medical Device Recall notice following the observation of a high risk that the needle electrode could ...

   Waarschuwing | 23-12-2021

4. Medtronic, Inc., FSN-FA948, ARESTM Antibiotic-Impregnated Catheter

   Medtronic roept vrijwillig specifieke partijen ARES™ met antibiotica geïmpregneerde shuntkatheters terug.

   Waarschuwing | 10-12-2020

5. Aesculap AG, FSN-FSCA249, AESCULAP AEOS

   With this letter Aesculap AG would like to inform you about a potential malfunction of product Aesculap Aeos®.

   Waarschuwing | 20-10-2020

6. Medtronic Inc. FA889 SynchroMed® II Implantable Infusion Pump

   Bij een permanente motorstop zal de medicamenteuze infusietherapie stoppen, wat kan leiden tot terugkeer van onderliggende ...

   Waarschuwing | 01-10-2019

7. Ad-Tech Medical 11-06-2019-00001 - Cortical Electrode, Depth Electrode, Anchor Bolt

   Ad-Tech Medical Instrument Corporation is recalling supplemental information that may have been sent to customers in response to ...

   Waarschuwing | 11-06-2019