NA 00-7711-013-20Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024131910), received between May 9, 2022 and Sep 1, 2022 — classified as 2 injuries.

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

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

Recent adverse event reports

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

• InjurySep 1, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT HAD A RIGHT TOTAL HIP ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT FELL GOING DOWN STAIRS AND SUSTAINED A PERIPROSTHETIC FRACTURE. THE PATIENT UNDERWENT AN OPEN REDUCTION OF THE FRACTURE, WITH CERCLAGE CABLES, ALONG WITH A REVISION OF THE RIGHT HIP APPROXIMATELY 1.5 MONTHS LATER. THE ACETABULAR COMPONENT REMAINED WELL FIXED AND ALL OTHER COMPONENTS WERE REVISED. NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Bone Fracture(s); Fall

  MAUDE report 15335618 ↗
• InjuryMay 9, 2022Migration; Migration

  IT WAS REPORTED THAT PATIENT WAS DIAGNOSED WITH AN IDIOPATHIC FRACTURE OF THE RIGHT HIP WITH STEM SUBSIDENCE CAUSING SEVERE PAIN AND DIFFICULTIES APPROXIMATELY 3 WEEKS POST RIGHT TOTAL HIP ARTHROPLASTY. NO INTERVENTION HAS BEEN REPORTED TO DATE, HOWEVER THE PATIENT SHOWS IMPROVEMENT WITH PAIN AND ABILITIES IN PHYSICIAN FOLLOW UP VISITS. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Ambulation or Postural Difficulties; Bone Fracture(s); Failure of Implant; Loss of Range of Motion; Pain

  MAUDE report 14336299 ↗

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