Home › Device types › MBH
Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
FDA product code MBH · Class 2 · Orthopedic
0
Registered devices
16,614
Adverse events
103
Recalls
146
510(k) clearances
Devices with this code
Scorpio — Howmedica Osteonics Corp.Klassic Femoral Augment, Distal — TOTAL JOINT ORTHOPEDICS, INC.PROPHECY — Microport Orthopedics Inc.Prophecy — Microport Orthopedics Inc.Klassic Tibial Baseplate with Ti-Coat, size 5 — TOTAL JOINT ORTHOPEDICS, INC.PROPHECY — Microport Orthopedics Inc.Optimotion Blue CR HCCR Total Knee System — OPTIMOTION IMPLANTS LLCProphecy — Microport Orthopedics Inc.Prophecy — Microport Orthopedics Inc.Prophecy — Microport Orthopedics Inc.Triathlon — Howmedica Osteonics Corp.VANGUARD KNEE SYSTEM — Biomet Orthopedics, LLCTRULIANT® — Exactech, Inc.PROPHECY — Microport Orthopedics Inc.PROPHECY — Microport Orthopedics Inc.PROPHECY — Microport Orthopedics Inc.PROPHECY — Microport Orthopedics Inc.PROPHECY® — Microport Orthopedics Inc.PROPHECY — Microport Orthopedics Inc.Prophecy — Microport Orthopedics Inc.Prophecy — Microport Orthopedics Inc.PERSONA® Vivacit-E® — Zimmer, Inc.Prophecy — Microport Orthopedics Inc.Triathlon — Howmedica Osteonics Corp.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-07-30 | Howmedica Osteonics Corp. | Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential f |
| 2026-05-19 | Howmedica 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 TY |
| 2026-05-19 | Howmedica 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 TY |
| 2026-05-11 | Zimmer, Inc. | Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package. |
| 2024-10-29 | MicroPort 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 packagin |
| 2024-03-13 | Biomet, Inc. | Possible damage to the Vanguard Knee System AS Tibial Bearing caused during the manufacturing process. |
| 2024-03-12 | DePuy Orthopaedics, Inc. | Product incorrectly labelled. |
| 2024-02-06 | Howmedica Osteonics Corp. | Potential packaging breaches of inner blister and outer sterile blister. |
| 2024-02-06 | Howmedica Osteonics Corp. | Potential packaging breaches of inner blister and outer sterile blister. |
| 2024-02-06 | Howmedica Osteonics Corp. | Potential packaging breaches of inner blister and outer sterile blister. |
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