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StageOne Select 431190Recalls & reported problems

Biomet Orthopedics, LLC · Class 2

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00880304521995), received between May 20, 2026 and May 20, 2026 — classified as 1 injury.

1 FDA recall record name this device's identifier.

14 other recalls cover devices cleared under the same FDA submission (K080979, K161166, K222760); 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. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 1 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Recalls naming this device

  1. Feb 26, 2020Terminated

    Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.

    Z-1643-2020 · Root cause: Process control · FDA record ↗

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Bone Fracture(s)1

Recent adverse event reports

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

  • InjuryMay 20, 2026Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED, APPROXIMATELY 8 MONTHS POSTOP, THE PATIENT PRESENTED WITH PERIPROSTHETIC INFECTION. A FIRST STAGE REVISION OCCURRED; ALL INITIAL IMPLANTS WERE REMOVED WITHOUT APPARENT COMPLICATION. AFTER REAMING THE FEMORAL CANAL, A NONDISPLACED FRACTURE IN THE PERITROCHANTERIC REGION WAS IDENTIFIED. AN UNKNOWN 3.5MM RECONSTRUCTION PLATE AND SCREWS WERE PLACED TO STABILIZE THE FRACTURE. NO FURTHER COMPLICATIONS WERE IDENTIFIED. FINAL INTRAOP X-RAYS INDICATED APPROPRIATE FRACTURE REDUCTION AND IMPLANT PLACEMENT. A CEMENT SPACER STEM WAS PLACED ALONG WITH AN ALL-POLY CUP, A CEMENTED CONSTRAINED LINER, AND ADDITIONAL SCREWS FOR FIXATION. DUE DILIGENCE IS IN PROGRESS FOR THIS COMPLAINT; TO DATE NO ADDITIONAL INFORMATION OR PRODUCT HAS BEEN RECEIVED.

    Patient problems: Bone Fracture(s)

    MAUDE report 25231005 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K080979, K161166, K222760. One submission often covers many models, so check the product and lot details in each record.

  • Z-1638-2020 · Feb 26, 2020 · Terminated
    BIOMET StageOne Hip Cement Spacer Mold with Insert, 48 MM, Silicone, Sterile, Item 431181.
  • Z-1644-2020 · Feb 26, 2020 · Terminated
    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 11 X 135 MM, Silicone, Sterile, Item 431191.
  • Z-1639-2020 · Feb 26, 2020 · Terminated
    BIOMET StageOne Hip Cement Spacer Mold with Insert, 52 MM, Silicone, Sterile, Item 431182.
  • Z-1650-2020 · Feb 26, 2020 · Terminated
    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 13 X 200 MM, Silicone, Sterile, Item 431197.
  • Z-1640-2020 · Feb 26, 2020 · Terminated
    BIOMET StageOne Hip Cement Spacer Mold with Insert, 56 MM, Silicone, Sterile, Item 431183.
  • Z-1645-2020 · Feb 26, 2020 · Terminated
    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 13 X 145 MM, Silicone, Sterile, Item 431192.
  • Z-1648-2020 · Feb 26, 2020 · Terminated
    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 9 X 200 MM, Silicone, Sterile, Item 431195.
  • Z-1642-2020 · Feb 26, 2020 · Terminated
    BIOMET StageOne Hip Cement Spacer Mold with Insert, 64 MM, Silicone, Sterile, Item 431185.
  • Z-1647-2020 · Feb 26, 2020 · Terminated
    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 17 X 165 MM, Silicone, Sterile, Item 431194.
  • Z-1649-2020 · Feb 26, 2020 · Terminated
    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 11 X 200 MM, Silicone, Sterile, Item 431196.
  • Z-1652-2020 · Feb 26, 2020 · Terminated
    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 17 X 200 MM, Silicone, Sterile, Item 431199.
  • Z-1641-2020 · Feb 26, 2020 · Terminated
    BIOMET StageOne Hip Cement Spacer Mold with Insert, 60 MM, Silicone, Sterile, Item 431184.
  • Z-1651-2020 · Feb 26, 2020 · Terminated
    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 15 X 200 MM, Silicone, Sterile, Item 431198.
  • Z-1646-2020 · Feb 26, 2020 · Terminated
    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 15 X 155 MM, Silicone, Sterile, Item 431193.

Other Prosthesis, hip, hemi-, femoral, metal devices

All Prosthesis, hip, hemi-, femoral, metal devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.