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NA 2357-101-14Recalls & reported problems

Zimmer, Inc. · Class 2 · Implant

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024055964), received between Aug 13, 2020 and Oct 21, 2021 — classified as 2 injuries.

The most frequently reported specific device problem is “Fracture” (2 reports).

4 other recalls cover devices cleared under the same FDA submission (K042598, 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 16, 2026.

Most reported problems

Device problems

  • Fracture2

Patient problems

  • Pain2
  • Adhesion(s)1
  • Bone Fracture(s)1
  • Failure of Implant1
  • Nonunion/Delayed-union Bone Fracture1
  • Osteopenia/ Osteoporosis1
  • Scar Tissue1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryOct 21, 2021Fracture; Fracture

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

    Patient problems: Adhesion(s); Bone Fracture(s); Failure of Implant; Nonunion/Delayed-union Bone Fracture; Osteopenia/ Osteoporosis; Pain; Scar Tissue

    MAUDE report 12676896 ↗
  • InjuryAug 13, 2020Fracture; Fracture

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

    Patient problems: Pain

    MAUDE report 10401211 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K042598, 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-0317-2020 · Oct 10, 2019 · Terminated
    Periarticular locking plate elbow-sterile, Item Nos. 47235800503 47235800509 47235800511 47235800515 47235800519 47235800603 47235800605 47235800607 47235800609 47235800611 4723580
  • 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-0646-2016 · Dec 9, 2015 · Terminated
    Zimmer Periarticular Locking Plate System 3.5mm Locking Screw 58 mm Length; Zimmer Periarticular Locking Plate System 2.4mm Locking Screw 14 mm Length. Indicated for temporary in

Other PLATE, FIXATION, BONE devices

All PLATE, FIXATION, BONE devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page