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HomeTOTAL JOINT ORTHOPEDICS, INC. › Modular Knee Impactor Head, Tibia

Modular Knee Impactor Head, Tibia

TOTAL JOINT ORTHOPEDICS, INC. · Model 2227.00.000 · UDI-DI 00819251024051

HWA Prescription
4
510(k) clearances
19,287
Adverse events
27
Recalls
303
Facilities

Description

Tibial Impactor Head

Recalls

DateFirmReason
2026-02-03Exactech, Inc.Impactor handle may be missing cross-pin
2026-02-03Exactech, Inc.Impactor handle may be missing cross-pin
2024-10-30INCIPIO DEVICESRecalled lot does not meet specification and has reported incidents of fracture of the TIG weld.
2023-06-05Exactech, Inc.The ball and spring housed within the locking mechanism of the handle can dislodge during disassembly or during impaction.
2020-05-12XTANT MedicalThe strike plate fractured off from the forceps inserter devices with minimal impaction or force due to unsatisfactory weld.
2019-08-16Enztec LimitedThe femoral impactors have a higher than normal risk of the arm breaking. During impaction the tip of the arm may fracture and separate from the instrument. This may cause a minor
2019-07-24Exactech, Inc.The threaded mechanism of the Threaded Offset Cup Impactor may be gritty and difficult to turn potentially due to entrapped blast media.
2017-08-28Zimmer Biomet, Inc.Potential for the Persona Partial Knee Impactor Pad to fracture.
2017-02-09Encore Medical, LpDuring the Turon assembly, the impaction forces caused the polymer, black acetal copolymer from the Impaction Fixture to wear off on the lateral surface of the Humeral Stem titaniu
2017-02-09Encore Medical, LpDuring the Turon assembly, the impaction forces caused the polymer, black acetal copolymer from the Impaction Fixture to wear off on the lateral surface of the Humeral Stem titaniu

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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.