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VerSys® 7871-13-61Recalls & reported problems

Zimmer, Inc. · Class 2 · Implant

All models of VerSys (41)

Data updated Oct 16, 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 00889024140035), received between Jun 29, 2023 and Jun 29, 2023 — classified as 1 injury.

5 other recalls cover devices cleared under the same FDA submission (K210842, K913649); 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 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Bone Fracture(s)1
  • Fall1
  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryJun 29, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

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

    Patient problems: Bone Fracture(s); Fall; Unspecified Infection

    MAUDE report 17229858 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K210842, K913649. One submission often covers many models, so check the product and lot details in each record.

  • Z-1166-2016 · Jan 11, 2016 · Terminated
    Product 68 consists of all product under product code: JDI and same usage: Item no: 787101360 VERSYS CEM/REV/CALCAR 13X 787101361 VERSYS CEM/REV/CALCAR 13X 787101362 VERSYS CEM/RE
  • Z-0608-2014 · Dec 10, 2013 · Terminated
    CPT Hip System, Parts 00-8114-002-10 and 00-8011-004-00 Hip joint metal/polymer semi-constrained cemented prosthesis. The CPT Hip System is indicated for cemented use in: Patients
  • Z-0610-2014 · Dec 10, 2013 · Terminated
    Versys Build-Up Block The VerSys CRC Hip System is indicated for total hip arthroplasty in patients whose bone stock is of poor quality or inadequate for other reconstruction tech
  • Z-1029-2014 · Oct 11, 2013 · Terminated
    12/14 UNIPOLAR FEMORAL HE VERSYS CEM LD/FX SZ 11X12 VERSYS CEM LD/FX SZ 12X12 VERSYS CEM LD/FX SZ 14X13 VERSYS CEM LD/FX SZ 16X14 VERSYS CEM LD/FX ST 18X15 VERSYS PRESS FIT LD/FX S
  • Z-0277-2014 · Aug 28, 2013 · Terminated
    VerSys Cemented Revision Calcar (CRC) Hip System Femoral Stems VerSys Heritage Hip System Revision Femoral Stems. Indicated for total hip arthroplasty.

Other Prosthesis, hip, semi-constrained, metal/polymer, cemented devices

All Prosthesis, hip, semi-constrained, metal/polymer, cemented devices →

Sources and updates

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