Devices

Device Recall Deltec PortACath

  • Modèle / numéro de série
    Lot M26982
  • 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 Low Profile Polysulfone/Titanium Venous Access System, Pre-assembled with PolyFlow Polyurethane Catheter, 1.9mm O.D. x 1.0mm I.D., 6 Fr Introducer Set, REF 21-4085-24
  • Manufacturer
    Deltec, Inc
  • 1 Event

Fabricant

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

18 dispositifs médicaux avec un nom similaire

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Device Recall Deltec PortACath
  • Modèle / numéro de série
    Lot M27052
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    3
  • Dispositif implanté ?
    No
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Description du dispositif
    Port-A-Cath II Low Profile Epidural Implantable Access System, with PolyFlow Polyurethane Catheter, 1.2mm O.D. x 0.5mm I.D., REF 21-1501-01
  • Manufacturer
    Deltec, Inc
Device Recall Deltec PortACath
  • Modèle / numéro de série
    Lot M27134
  • 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 Titanium Venous Access System, with Silicone Catheter, 2.8mm O.D. x 1.0mm I.D., 9 Fr Introducer Set, REF 21-4009-24
  • Manufacturer
    Deltec, Inc
Device Recall Deltec PortACath
  • Modèle / numéro de série
    Lot M27051
  • 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 Low Profile Titanium Venous Access System, with Silicone Catheter, 2.8mm O.D. x 1.0mm I.D., 9 Fr Introducer Set, REF 21-4035-24
  • Manufacturer
    Deltec, Inc
Device Recall Deltec PortACath
  • Modèle / numéro de série
    Lots M27118 and M27262
  • 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 Low Profile Titanium Venous Access System, with PolyFlow Polyurethane Catheter, 1.9mm O.D. x 1.0mm I.D., 6 Fr Introducer Set, REF 21-4037-24
  • Manufacturer
    Deltec, Inc
Device Recall Deltec PortACath
  • Modèle / numéro de série
    Lot M27037
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Description du dispositif
    Port-A-Cath II Epidural Low Profile Polysulfone/Titanium Access System, with PolyFlow Polyurethane Catheter, 1.2mm O.D. x 5mm I.D., REF 21-1501-22
  • Manufacturer
    Deltec, Inc
13 en plus