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
Recalls naming this device
- 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 · TerminatedBIOMET StageOne Hip Cement Spacer Mold with Insert, 48 MM, Silicone, Sterile, Item 431181.
- Z-1644-2020 · Feb 26, 2020 · TerminatedBIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 11 X 135 MM, Silicone, Sterile, Item 431191.
- Z-1639-2020 · Feb 26, 2020 · TerminatedBIOMET StageOne Hip Cement Spacer Mold with Insert, 52 MM, Silicone, Sterile, Item 431182.
- Z-1650-2020 · Feb 26, 2020 · TerminatedBIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 13 X 200 MM, Silicone, Sterile, Item 431197.
- Z-1640-2020 · Feb 26, 2020 · TerminatedBIOMET StageOne Hip Cement Spacer Mold with Insert, 56 MM, Silicone, Sterile, Item 431183.
- Z-1645-2020 · Feb 26, 2020 · TerminatedBIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 13 X 145 MM, Silicone, Sterile, Item 431192.
- Z-1648-2020 · Feb 26, 2020 · TerminatedBIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 9 X 200 MM, Silicone, Sterile, Item 431195.
- Z-1642-2020 · Feb 26, 2020 · TerminatedBIOMET StageOne Hip Cement Spacer Mold with Insert, 64 MM, Silicone, Sterile, Item 431185.
- Z-1647-2020 · Feb 26, 2020 · TerminatedBIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 17 X 165 MM, Silicone, Sterile, Item 431194.
- Z-1649-2020 · Feb 26, 2020 · TerminatedBIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 11 X 200 MM, Silicone, Sterile, Item 431196.
- Z-1652-2020 · Feb 26, 2020 · TerminatedBIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 17 X 200 MM, Silicone, Sterile, Item 431199.
- Z-1641-2020 · Feb 26, 2020 · TerminatedBIOMET StageOne Hip Cement Spacer Mold with Insert, 60 MM, Silicone, Sterile, Item 431184.
- Z-1651-2020 · Feb 26, 2020 · TerminatedBIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 15 X 200 MM, Silicone, Sterile, Item 431198.
- Z-1646-2020 · Feb 26, 2020 · TerminatedBIOMET 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
- UHR UH1-48-28Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal2 recalls3 reports
- "UNITED" USTAR II Knee System 2515-3213United Orthopedic Corp. · Prosthesis, Hip, Hemi-, Femoral, Metal2 recalls0 reports
- "UNITED" USTAR II Knee System 2515-3115United Orthopedic Corp. · Prosthesis, Hip, Hemi-, Femoral, Metal2 recalls0 reports
- STAGEONE 431207Biomet Orthopedics, LLC · Prosthesis, hip, hemi-, femoral, metal2 recalls0 reports
- "UNITED" USTAR II Knee System 2515-3111United Orthopedic Corp. · Prosthesis, Hip, Hemi-, Femoral, Metal2 recalls0 reports
- ACTIS 101011050Depuy (Ireland) · Prosthesis, hip, hemi-, femoral, metal73 reports
- UHR UH1-46-26Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal1 recall11 reports
- UHR UH1-45-26Howmedica Osteonics Corp. · Prosthesis, hip, hemi-, femoral, metal1 recall11 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.