Persona® 42-5099-090-00Recalls & reported problems
Zimmer, Inc. · Class 1
- Adverse event reports
- 18
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 18 adverse event reports that list this exact device (DI 00880304809352), received between Mar 22, 2021 and Aug 6, 2026 — classified as 18 malfunctions.
The most frequently reported specific device problem is “Fracture” (18 reports).
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
Most reported problems
Device problems
- Fracture18
- Naturally Worn2
Patient problems
- No Clinical Signs, Symptoms or Conditions18
Recent adverse event reports
The 18 most recent of 18 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 6, 2026Fracture; Naturally Worn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50155603 ↗MalfunctionAug 6, 2026Fracture; Naturally Worn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50155209 ↗MalfunctionApr 2, 2026Fracture
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24768055 ↗MalfunctionOct 31, 2025Fracture; Fracture
NO FURTHER EVENT INFORMATION AT TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23435194 ↗MalfunctionOct 1, 2024Fracture; Fracture
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20343469 ↗MalfunctionSep 16, 2024Fracture; Fracture
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20226294 ↗MalfunctionApr 3, 2024Fracture; Fracture
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19036883 ↗MalfunctionNov 21, 2023Fracture; Fracture
NO FURTHER EVENT INFORMATION AT TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18184018 ↗MalfunctionAug 24, 2023Fracture; Fracture
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17612146 ↗MalfunctionJul 20, 2023Fracture; Fracture
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17362132 ↗MalfunctionApr 19, 2023Fracture; Fracture
IT WAS REPORTED THAT THE PERSONA PARTIAL KNEE LOCKING FEMORAL IMPACTOR PAD BROKE DURING SURGERY. THE SURGICAL TECHNIQUE WAS UTILIZED. THERE WAS NO SURGICAL DELAY. NO FOREIGN BODIES WERE RETAINED. THE SURGERY WAS NOT COMPLETED WITH A SECOND DEVICE. ALL AVAILABLE INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16770921 ↗MalfunctionFeb 27, 2023Fracture; Fracture
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16443700 ↗MalfunctionMay 13, 2022Fracture; Fracture
IT WAS REPORTED DURING A KNEE ARTHROPLASTY THAT THE IMPACTOR PAD FRACTURED WHILE IMPACTING THE FEMORAL COMPONENT. THE PROCEDURE WAS COMPLETED UTILIZING ANOTHER IMPACTOR WITHOUT ANY FURTHER COMPLICATIONS. NO ADVERSE EVENTS WERE REPORTED AS A RESULT OF THIS MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14397938 ↗MalfunctionApr 5, 2022Fracture; Fracture
IT WAS REPORTED THAT A FEMORAL IMPACTOR PAD WAS FOUND TO BE FRACTURED. IT WAS REPORTED THAT THERE WAS NO PATIENT INVOLVEMENT AND THAT NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14014398 ↗MalfunctionMar 31, 2022Fracture; Fracture
IT WAS REPORTED THE BLUE FEMORAL IMPACTOR BROKE IN HALF WHILE IMPACTING FEMORAL TRIAL. ATTEMPTS HAVE BEEN MADE TO OBTAIN ADDITIONAL INFORMATION, HOWEVER, NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13967872 ↗MalfunctionMar 8, 2022Fracture; Fracture
IT WAS REPORTED THAT THE IMPACTOR FRACTURED DURING A KNEE PROCEDURE. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13695981 ↗MalfunctionSep 7, 2021Fracture; Fracture
UPON REASSESSMENT OF THE REPORTED EVENT, IT WAS DETERMINED AN MDR SHOULD NOT HAVE BEEN FILED UNDER THE CURRENT MFR NUMBER. THIS EVENT WILL BE REPORTED ON 0001825034-2022-00495.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12433303 ↗MalfunctionMar 22, 2021Fracture; Fracture
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11543394 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.