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HomeTOTAL JOINT ORTHOPEDICS, INC. › Klassic Tibial Insert, PS-Max, Std Poly

Klassic Tibial Insert, PS-Max, Std Poly

TOTAL JOINT ORTHOPEDICS, INC. · Model 6300.03.011 · UDI-DI 00819251028103

MBHJWH Prescription
1
510(k) clearances
16,331
Adverse events (11 deaths)
102
Recalls
217
Facilities

Description

Tibial Insert, PS-Max, Std Poly, Size 3, 11mm

Recalls

DateFirmReason
2026-05-19Howmedica Osteonics Corp.Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon
2026-05-19Howmedica Osteonics Corp.Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon
2026-05-11Zimmer, Inc.Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.
2024-10-29MicroPort Orthopedics Inc.Femoral implant porous size 5 right primary and femoral implant non-porous size 6 left primary have correct markings on devices, but may have incorrect packaging.
2024-03-13Biomet, Inc.Possible damage to the Vanguard Knee System AS Tibial Bearing caused during the manufacturing process.
2024-03-12DePuy Orthopaedics, Inc.Product incorrectly labelled.
2024-02-06Howmedica Osteonics Corp.Potential packaging breaches of inner blister and outer sterile blister.
2024-02-06Howmedica Osteonics Corp.Potential packaging breaches of inner blister and outer sterile blister.
2024-02-06Howmedica Osteonics Corp.Potential packaging breaches of inner blister and outer sterile blister.
2024-02-06Howmedica Osteonics Corp.Potential packaging breaches of inner blister and outer sterile blister.

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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.