NA 2357-09-08Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024055773), received between Jun 5, 2020 and Jun 5, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Material Discolored” (1 report).

3 other recalls cover devices cleared under the same FDA submission (K050121, K141734); 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.

• InjuryJun 5, 2020Material Discolored; Material Discolored

  NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Tissue Damage; Unspecified Infection

  MAUDE report 10123059 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K050121, K141734. One submission often covers many models, so check the product and lot details in each record.

• Z-2254-2023 · Jun 27, 2023 · Open, Classified
  Zimmer Periarticular Locking Plate (ZPLP) Distal Lateral Femoral Plate 6 holes 159 mm Length-Indicated for temporary internal fixation and stabilization of osteotomies and fracture
• Z-0310-2020 · Oct 10, 2019 · Terminated
  DIST LAT FEM LCK PLATE STERILE, Item Nos. 47235710106 47235710110 47235710114 47235710118 47235710122 47235710210 47235710214 47235710218 47235710222
• Z-0317-2020 · Oct 10, 2019 · Terminated
  Periarticular locking plate elbow-sterile, Item Nos. 47235800503 47235800509 47235800511 47235800515 47235800519 47235800603 47235800605 47235800607 47235800609 472358006