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Persona® Vivacit-E® 42-5128-004-24Recalls & reported problems

Zimmer, Inc. · Class 2 · Implant

All models of PERSONA Vivacit-E (285)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024554115), received between May 26, 2022 and May 26, 2022 — classified as 1 injury.

1 other recall cover devices cleared under the same FDA submission (K181947, K191625); 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

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Pain1
  • Swelling/ Edema1

Recent adverse event reports

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

  • InjuryMay 26, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE PATIENT WAS TREATED WITH AN INJECTION FOR PES BURSITIS APPROXIMATELY SEVENTEEN (17) MONTHS FOLLOWING A LEFT KNEE ARTHROPLASTY TO ADDRESS CONTINUOUS POST-OPERATIVE PAIN AND SWELLING. THE PATIENT'S PAIN RESOLVED AFTER THE INJECTION WAS ADMINISTERED, HOWEVER, THE PATIENT CONTINUED TO HAVE WORSENING MODERATE EFFUSION. INITIAL OPERATIVE NOTES NOTED THAT THE PARTIAL KNEE ARTHROPLASTY TRACKED WITHOUT COMPLICATION AND THE PATIENT'S RANGE OF MOTION WAS ZERO (0) TO ONE-HUNDRED FORTY(140) DEGREES AND STABLE. ATTEMPTS HAVE BEEN MADE, HOWEVER, NO ADDITIONAL INFORMATION IS AVAILABLE.

    Patient problems: Pain; Swelling/ Edema

    MAUDE report 14517258 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K181947, K191625. One submission often covers many models, so check the product and lot details in each record.

  • Z-2578-2026 · May 11, 2026 · Open, Classified
    Brand Name: Persona Revision Product Name: Persona Revision Trabecular Metal Femoral Distal Augment Model/Catalog Number: 42-5572-066-10 Software Version: N/A Product Description:

Other PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER devices

All PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page