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NA 00-7711-006-10Recalls & reported problems

Zimmer, Inc. · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024131675), received between May 4, 2021 and Jul 6, 2022 — classified as 1 injury, 1 malfunction.

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

3 other recalls cover devices cleared under the same FDA submission (K032726, K192660); 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

Device problems

  • Adverse Event Without Identified Device or Use Problem1
  • Corroded1
  • Material Erosion1
  • Packaging Problem1

Patient problems

  • Metal Related Pathology1
  • Muscle/Tendon Damage1
  • No Clinical Signs, Symptoms or Conditions1
  • Pain1

Recent adverse event reports

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

  • MalfunctionJul 6, 2022Packaging Problem; Packaging Problem

    IT WAS REPORTED THAT THE STERILE PACKAGE WAS DAMAGED. NO ADVERSE EVENTS HAVE BEEN REPORTED AS A RESULT OF THE MALFUNCTION AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14933584 ↗
  • InjuryMay 4, 2021Corroded; Material Erosion; Adverse Event Without Identified Device or Use Problem; Corroded; Material Erosion; Adverse Event Without Identified Device or Use Problem

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

    Patient problems: Metal Related Pathology; Muscle/Tendon Damage; Pain

    MAUDE report 11772994 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K032726, K192660. One submission often covers many models, so check the product and lot details in each record.

  • Z-1191-2018 · Mar 1, 2018 · Terminated
    Zimmer M/L Taper Hip Prosthesis, 7711 Series, Femoral Stem 12/14 Neck Taper Plasma Sprayed Press-Fit Cementless Size 7.5 Extended Offset Reduced Neck Length; Part Number: 00-7711-0
  • Z-1046-2016 · Feb 11, 2016 · Terminated
    M/L Taper Hip Prosthesis (Item: 00-7711-012-20, Lot: 62937093
  • Z-2033-2014 · May 23, 2014 · Terminated
    Zimmer M/L Taper Hip Stem Standard & Extended Offset, HIP JOINT PROSTHESIS, Sizes: 5.0, 7.5, 9.0, 10.0, 11.0, 12.5, 13.5, 15.0, 11.25, 17.25, 20.0 & 22.5. The femoral stem com

Other Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices

All Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices →

Sources and updates

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