MP Reconstruction Prosthesis 172-918/16Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04026575320615), received between Apr 19, 2023 and Apr 19, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

2 other recalls cover devices cleared under the same FDA submission (K142187); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryApr 19, 2023Insufficient Device Problem Information; Insufficient Device Problem Information

  AN MP MODULAR STEM SYSTEM, ORIGINALLY IMPLANTED ON (B)(6) 2021, WAS REVISED BECAUSE OF INFECTION. THE IMPLANTS WERE REMOVED AND REPLACED WITH AN ANTIBIOTIC SPACER.

  Patient problems: Medical device site infection

  MAUDE report 16770520 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K142187. One submission often covers many models, so check the product and lot details in each record.

• Z-0769-2025 · Dec 5, 2024 · Open, Classified
  LINK MP Reconstruction System Neck Segment (with suture holes, standard, uncemented, L= 35 mm, CCD 126, Offset= 31 mm, Ti6Al4V, PoroLink, Taper 12/14. Item Number: 99-0984/32 I
• Z-0733-2019 · Dec 7, 2018 · Terminated
  LINK STEM with Microporous Surface MP Reconstruction Prosthesis, CEMENTLESS (Size XS-0, D: 12mm, L: 160mm), Reference Number 172-916/12 Product Usage: The LINK STEM with Microp