Devices

Device Recall Triathlon

  • Model / Serial
    Catalog Number: I-K2401KF00 (note each is uniquely identified/marked as IK2401KF0L and IK2401KF0R - Left and Right).   Lot Codes: AP5W52 and AP7H19.
  • Product Classification
    Orthopedic Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    1 Branch (NJ) with one consignee (DE).
  • Product Description
    Howmedica Osteonics Corp. Stryker Orthopaedics Specialty Triathlon Left and Right A//P Sizer Adjustment Housing PER File K2401. For use in knee prosthesis implantation. NON-STERILE
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
  • 1 Event

Manufacturer

Stryker Howmedica Osteonics Corp.
  • Manufacturer Address
    Stryker Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah NJ 07430
  • Manufacturer Parent Company (2017)
    Stryker
  • Source
    USFDA

36 devices with a similar name

Learn more about the data here

Device Recall Triathlon X3
  • Model / Serial
    Product numbers: 5537-G-109, 5537-G-111, 5537-G-113, 5537-G-116, 5537-G-119, 5537-G-122, 5537-G-125, 5537-G-128, 5537-G-131, 5537-G-209, 5537-G-211, 5537-G-213, 5537-G-216, 5537-G-219, 5537-G-222, 5537-G-225, 5537-G-228,  5537-G-231, 5537-G-309, 5537-G-311, 5537-G-313, 5537-G-316, 5537-G-319, 5537-G-322, 5537-G-325, 5537-G-328, 5537-G-331, 5537-G-409, 5537-G-411, 5537-G-413, 5537-G-416, 5537-G-419, 5537-G-422, 5537-G-425, 5537-G-428, 5537-G-431, 5537-G-509, 5537-G-511, 5537-G-513, 5537-G-516, 5537-G-519, 5537-G-522, 5537-G-525, 5537-G-528, 5537-G-531, 5537-G-609, 5537-G-611, 5537-G-613, 5537-G-616, 5537-G-619, 5537-G-622, 5537-G-625, 5537-G-628, 5537-G-631, 5537-G-709, 5537-G-711, 5537-G-713, 5537-G-716, 5537-G-719, 5537-G-722, 5537-G-725, 5537-G-728, 5537-G-731, 5537-G-809, 5537-G-811, 5537-G-813, 5537-G-816, 5537-G-819, 5537-G-822, 5537-G-825, 5537-G-828, 5537-G-831.  All lot codes
  • Product Classification
    Orthopedic Devices
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Product distributed to 5 hospitals in GA, OH, MN, TX.
  • Product Description
    Triathlon X3 || Total Stabilizer + Tibial Insert || For use with Triathlon Universal Baseplates, knee prosthesis. || #5 13mm || Stryker Orthopaedics
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
Device Recall Triathlon Baseplate Impactor Extractor
  • Model / Serial
    Catalog Number 6541-4-805 Lot Code NYC08
  • Product Classification
    Orthopedic Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution
  • Product Description
    Triathlon Baseplate Impactor Extractor, Orthopedic manual surgical instrument, Catalog Number 6541-4-805, Non-Sterile, Stryker Howmedica Osteonics Corp, Mahwah, NJ 07430
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
Device Recall Triathlon TS Femoral Trial
  • Model / Serial
    Lot codeL WFLD
  • Product Classification
    Orthopedic Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
  • Product Description
    Triathlon TS Femoral Trial; || Size 1 Left || Non-Sterile || Catalog number 5512-T-101 || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || Orthopedic Manual Surgical Instrument indicated for use in revision Total Knee Arthroplasty.
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
Device Recall Triathlon TS Femoral Trial
  • Model / Serial
    Lot Code WFLI
  • Product Classification
    Orthopedic Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
  • Product Description
    Triathlon TS Femoral Trial; || Size 1 Right || Non-Sterile || Catalog number: 5512-T-102 || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || Orthopedic Manual Surgical Instrument indicated for use in revision Total Knee Arthroplasty.
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
Device Recall Triathlon TS Femoral Trial
  • Model / Serial
    Lot code WFLV
  • Product Classification
    Orthopedic Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
  • Product Description
    Triathlon TS Femoral Trial; || Size 2 Left || Non-Sterile || Catalog Number 5512-T-201 || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || Orthopedic Manual Surgical Instrument indicated for use in revision Total Knee Arthroplasty.
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
31 more