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Tracker Plus Kyphoplasty System

GS Medical Co., Ltd. · Model GSFB-1120 · UDI-DI 08809695579769

NDNHRX Prescription
1
510(k) clearances
4,809
Adverse events (94 deaths)
86
Recalls
114
Facilities

Recalls

DateFirmReason
2022-12-15TEKNIMED SASIncorrect expiry date. Product is labeled with expiry date 2027-02-28. The correct expiration date is 2025-02-28.
2021-05-18Stryker SpineThe products experienced a 12-hour excursion from the required refrigerated temperature conditions at the distribution center prior to distribution.
2021-05-18Stryker SpineThe products experienced a 12-hour excursion from the required refrigerated temperature conditions at the distribution center prior to distribution.
2021-03-25ZavationProducts distributed as sterile may not have been adequately sterilized
2021-03-25ZavationProducts distributed as sterile may not have been adequately sterilized
2021-03-25ZavationProducts distributed as sterile may not have been adequately sterilized
2021-03-25ZavationProducts distributed as sterile may not have been adequately sterilized
2021-03-25ZavationProducts distributed as sterile may not have been adequately sterilized
2021-03-25ZavationProducts distributed as sterile may not have been adequately sterilized
2021-03-25ZavationProducts distributed as sterile may not have been adequately sterilized

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.