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NA 00-7711-009-20Recalls & reported problems

Zimmer, Inc. · Class 2 · Implant

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024131767), received between Oct 21, 2021 and Oct 21, 2021 — classified as 1 injury.

3 other recalls cover devices cleared under the same FDA submission (K032726, K161830, 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

Patient problems

  • Pain1

Recent adverse event reports

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

  • InjuryOct 21, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED WAS REPORTED PATIENT RETURNED TO HOSPITAL 3 YEARS POST IMPLANTATION DUE TO RIGHT THIGH PAIN THAT RADIATES TO HIP. THE SURGEON IS UNCERTAIN IF THE EVENT IS RELATED TO THE DEVICE. TREATED INITIALLY WITH CONSERVATIVE MONITORING, BUT SINCE PAIN IS PERSISTENT, IMAGING AND BONE SCAN TAKEN WITH RESULTS PENDING AT TIME OF REPORTING. PATIENT REPORTS CONTINUED SEVERE PAIN. ALL WORKUP FOR INFECTION HAVE BEEN NEGATIVE AND REASONS FOR THE PAIN THUS FAR INCONCLUSIVE. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

    Patient problems: Pain

    MAUDE report 12671444 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K032726, K161830, 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/POLYMER, POROUS UNCEMENTED devices

All PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices →

Sources and updates

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