Devices

Device Recall Deltec PortACath II

  • Modèle / numéro de série
    Lots M26975 and M27127
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Description du dispositif
    Port-A-Cath II Dual-lumen Low Profile Polysulfone/Titanium Venous Access System, with Dual-lumen PolyFlow Polyurethane Catheter, 2.2mm O.D. x 1.0mm I.D., 7 French Introducer Set, REF 21-8066-24
  • Manufacturer
    Deltec, Inc
  • 1 Event

Fabricant

Deltec, Inc
  • Adresse du fabricant
    Deltec, Inc, 1265 Grey Fox Rd, Saint Paul MN 55112-6929
  • Source
    USFDA

2 dispositifs médicaux avec un nom similaire

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Device Recall Deltec PortACath II FluoroFree
  • Modèle / numéro de série
    Lot M27047
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Description du dispositif
    Port-A-Cath II Fluoro-Free Low Profile Venous Access System, with PolyFlow Polyurethane Catheter, 2.6mm O.D. x 1.6mm I.D., and with CATH-FINDER Sensor Wire, REF 21-4685-24
  • Manufacturer
    Deltec, Inc
Device Recall Deltec PortACath II
  • Modèle / numéro de série
    Lot M26983
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Description du dispositif
    Port-A-Cath II Dual-lumen Low Profile Polysulfone/Titanium Venous Access System, with Dual-lumen PolyFlow Polyurethane Catheter, 3.2mm O.D. x 1.4mm I.D., 10 French Introducer Set, REF 21-8068-24
  • Manufacturer
    Deltec, Inc