ZMR® 9923-78-45Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024157279), received between Nov 14, 2023 and Jun 25, 2024 — classified as 2 injuries.

The most frequently reported specific device problem is “Inadequacy of Device Shape and/or Size” (1 report).

6 other recalls cover devices cleared under the same FDA submission (K031572, K113296); 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.

• InjuryJun 25, 2024Off-Label Use; Adverse Event Without Identified Device or Use Problem; Off-Label Use; Adverse Event Without Identified Device or Use Problem

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

  Patient problems: Numbness; Pain

  MAUDE report 19608920 ↗
• InjuryNov 14, 2023Inadequacy of Device Shape and/or Size; Inadequacy of Device Shape and/or Size

  IT WAS REPORTED A PATIENT UNDERWENT A HIP REVISION DUE TO A LIMB LENGTH DISCREPANCY. THERE WAS NO HARM OR COMPLICATIONS TO WITH THE PATIENT. ONLY A CORRECTION TO THE LENGTH OF THE LIMB. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Unequal Limb Length

  MAUDE report 18129418 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K031572, K113296. One submission often covers many models, so check the product and lot details in each record.

• Z-2582-2017 · Feb 28, 2017 · Terminated
  Xl por st 24.0x220mm, bowed, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants
• Z-2583-2017 · Feb 28, 2017 · Terminated
  Xl por st 25.5x220mm, bowed\, bowed, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants
• Z-0324-2012 · Oct 21, 2011 · Terminated
  ZMR Over the Junction Instruments for Revision, utilized for the following ZMR devices: Porous Stem,Nitrited Porous Revision, Slotted Porous Bowed Stems with and without Compressio
• Z-0323-2012 · Oct 21, 2011 · Terminated
  ZMR Crossover Instrumentation, utilized for the following ZMR devices: Porous Stem,Nitrited Porous Revision, Slotted Porous Bowed Stems with and without Compression Nut, Splined St
• Z-0322-2012 · Oct 21, 2011 · Terminated
  ZMR Porous Revision Hip Prosthesis Surgical Technique, utilized for the following ZMR devices: Porous Stem,Nitrited Porous Revision, Slotted Porous Bowed Stems with and without Com
• Z-0321-2012 · Oct 21, 2011 · Terminated
  Zimmer ZMR Hip System Instructions for Use, utilized for the following ZMR devices: Porous Stem,Nitrited Porous Revision, Slotted Porous Bowed Stems with and without Compression Nu