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Crédits
Devices
Device Recall Triathlon
Modèle / numéro de série
Ref. No. 5530-G-211 Lot code G9XF6 LAF974
Classification du dispositif
Orthopedic Devices
Classe de dispositif
2
Dispositif implanté ?
Yes
Distribution
Nationwide and Canada.
Description du dispositif
Triathlon X3 CR Tibial Bearing Insert || for knee prosthesis || Size #2 - 11MM || Ref # 5530-G-211 || 2011-09 || Howmedica Osteonics Corp.
Manufacturer
Stryker Howmedica Osteonics Corp.
1 Event
Rappel de Device Recall Triathlon
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Fabricant
Stryker Howmedica Osteonics Corp.
Adresse du fabricant
Stryker Howmedica Osteonics Corp., 325 Corporate Dr, Mahwah NJ 07430-2002
Société-mère du fabricant (2017)
Stryker
Source
USFDA
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Device Recall Triathlon X3
Modèle / numéro de série
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
Classification du dispositif
Orthopedic Devices
Classe de dispositif
2
Dispositif implanté ?
Yes
Distribution
Product distributed to 5 hospitals in GA, OH, MN, TX.
Description du dispositif
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
Modèle / numéro de série
Catalog Number 6541-4-805 Lot Code NYC08
Classification du dispositif
Orthopedic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Worldwide Distribution
Description du dispositif
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
Modèle / numéro de série
Lot codeL WFLD
Classification du dispositif
Orthopedic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
Description du dispositif
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
Modèle / numéro de série
Lot Code WFLI
Classification du dispositif
Orthopedic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
Description du dispositif
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
Modèle / numéro de série
Lot code WFLV
Classification du dispositif
Orthopedic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
Description du dispositif
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.
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