Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen

1. Brainlab AG, CAPA-20190904-002337, Patient Data Manager

   Onder specifieke omstandigheden kan dit probleem ertoe leiden dat verschuivingen in segmentatieobjecten in iPlan niet worden ...

   Waarschuwing | 08-10-2019

2. Ethicon Endo-Surgery LLC FMJR 19-058 ECHELON FLEX™ Powered Plus ENDOPATH® 60mm Stapler – 340mm shaft

   Ethicon has initiated a voluntary recall of specific product lots and kits of ECHELON FLEX ENDOPATH 60mm Staplers, were ...

   Waarschuwing | 08-10-2019

3. Teleflex Medical EIF-000369 DispoGrip

   Teleflex Medical is issuing a Field Safety Advisory Notice for the product referenced above due to a labelling error on the outer ...

   Waarschuwing | 06-09-2019

4. Olympus Medical Systems, QIL 152-005, MAJ-209 SINGLE USE SUCTION VALVE

   As of today, and as a mere, additional precautionary measure, Olympus is enabled for a proper and timely replacement of the ...

   Waarschuwing | 28-08-2019

5. Ethicon Endo Surgery 19-043 update - Curved Intraluminal Staplers (ILS)

   In april jl. informeerden wij u dat Ethicon Endo-Surgery, LLC. ("Ethicon") een kennisgeving voor meerdere lotnummers van het ...

   Waarschuwing | 01-08-2019

6. Teleflex Medical, EIF-000360, Auto Endo5 ML

   Teleflex roept het hierboven genoemde product terug, omdat er variabele gegevens kunnen ontbreken op het label dat op elke unit ...

   Waarschuwing | 24-05-2019

7. Olympus, QIL 152-002, EVIS EXERA(Q190V)-/LUCERA(Q290V) DUODENOVIDEOSCOPE

   Our early warning system has recently signaled an increase in the number of complaints from customers who noticed air leakage ...

   Waarschuwing | 10-05-2019

8. Olympus Medical Systems Corporation, QIL 152-001, OLYMPUS Duodenovideoscope

   Olympus has received complaints about fraying elevator wires of the TJF-160VR, but these complaints have not resulted in any ...

   Waarschuwing | 07-05-2019

9. Ethicon Endo-Surgery FMJR_19-026 - Intraluminal Staplers (ILS)

   Door onderzoek van klachten en geretourneerde producten blijkt dat niet gesneden sluitringen (washers) en misvormde staples ...

   Waarschuwing | 01-04-2019

10. ConMed Corporation, MDSS ref.: MDD19.090, Anchor Tissue Retrieval System™

    CONMED has received complaints that the individual device pouch had a void in its seal.

    Waarschuwing | 20-03-2019