Device Recall Optimus

  • Model / Serial
    serial #s - G15733, G15704, G15729, G14262, G15750, G15500, G15726, G14065, G15516, G15622, G14118, G14504, G15525, G15551, G14444, G14445, G14406, G15810, G15855, G16651, G16167, G15861, G15858, G15921, G15974, G16132, G16567, G16678, G17593, G16259, G16146, G16573, G17052, G17556, G17504, G16347, G17520, G17506, G17400, G17773, G17774, G17403, G16393. One unit identified with site #103950.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Devices were distributed to 38 medical centers and hospitals throughout the US.
  • Product Description
    Optimus 30
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Philips Ultrasound, Inc., 22100 Bothell-Everett Hwy., P.O. Box 3003, Bothell WA 98041-3003
  • Source
    USFDA

One device with a similar name

Learn more about the data here

  • Model / Serial
    Part Number 139005 - Lot Number 182-16146
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    US Distribution to the states of : FL, GA. IL, MO, TX
  • Product Description
    Optimus Fixed Awl
  • Manufacturer