Devices

Device Recall JOURNEY " UNI TIBIAL INSERT LEFT MEDIAL/RIGHT LATERAL

  • Model / Serial
    All Lot Numbers
  • Product Classification
    Orthopedic Devices
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    US and Argentina, Switzerland, Australia, Canada, Belgium, Italy, Spain, Thailand, Austria; PROC, Finland, Germany, Malaysia, Portugal, Netherlands, Singapore, and England
  • Product Description
    JOURNEY " UNI TIBIAL INSERT LEFT MEDIAL/RIGHT LATERAL, A/P 38 MM, M/L 24 MM, REF 71422243, QTY: (1), STERILE EO, SMITH & NEPHEW, INC. MEMPHIS, TN 38116
  • Manufacturer
    Smith & Nephew Inc
  • 1 Event

Manufacturer

Smith & Nephew Inc
  • Manufacturer Address
    Smith & Nephew Inc, 1450 E. Brooks Rd, Memphis TN 38116
  • Manufacturer Parent Company (2017)
    Smith & Nephew plc
  • Source
    USFDA

One device with a similar name

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Device Recall JOURNEY " UNI TIBIAL INSERT LEFT MEDIAL/RIGHT LATERAL,
  • Model / Serial
    All Lot Numbers
  • Product Classification
    Orthopedic Devices
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    US and Argentina, Switzerland, Australia, Canada, Belgium, Italy, Spain, Thailand, Austria; PROC, Finland, Germany, Malaysia, Portugal, Netherlands, Singapore, and England
  • Product Description
    JOURNEY " UNI TIBIAL INSERT LEFT MEDIAL/RIGHT LATERAL, A/P 38 MM, M/L 24 MM, REF 71422244, QTY: (1), STERILE EO, SMITH & NEPHEW, INC. MEMPHIS, TN 38116
  • Manufacturer
    Smith & Nephew Inc