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VerSys® 8018-22-02Recalls & 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
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024144538), received between May 5, 2022 and Jul 11, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (2 reports).

23 other recalls cover devices cleared under the same FDA submission (K840643, K953337); 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

  • Device Dislodged or Dislocated2

Patient problems

  • Joint Dislocation2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryJul 11, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

    NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

    Patient problems: Joint Dislocation

    MAUDE report 17297971 ↗
  • InjuryMay 5, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

    IT WAS REPORTED THAT THE PATIENT WAS REVISED DUE TO HIP DISLOCATION AND DISASSOCIATION OF THE HEAD AND BEARING APPROXIMATELY 4 YEARS POST IMPLANTATION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

    Patient problems: Joint Dislocation

    MAUDE report 14291769 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K840643, K953337. One submission often covers many models, so check the product and lot details in each record.

  • Z-0722-2018 · Aug 1, 2017 · Terminated
    Versys 6 inch Beaded Full Coat Plus Hip Prosthesis. Labeled as follows: a. VERSYS 6 INCH BEADED FC 19X160MM STD BODY STD NECK (Item No. 00894301906); b. VERSYS 6 INCH BEADED F
  • Z-2579-2017 · Feb 28, 2017 · Terminated
    Por fullct fem st 17x200mm, Sterile,
  • Z-2580-2017 · Feb 28, 2017 · Terminated
    Por fullct fem st 18x200mm, Sterile,
  • Z-2578-2017 · Feb 28, 2017 · Terminated
    Por fullct fem st 16x200mm, Sterile,
  • Z-2581-2017 · Feb 28, 2017 · Terminated
    Por fullct fem st 20x200mm, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants
  • Z-2577-2017 · Feb 28, 2017 · Terminated
    Por fullct fem st 15x200mm, Sterile, prosthesis, hip, semi-constrained, metal/polymer, porous uncemented- Specific Knee, Hip and Nail Implants
  • Z-1683-2016 · May 4, 2016 · Terminated
    Hgp ii acetabular cup bone screw selftap 6.5x15mm 00662406515 Hgp ii acetabular cup bone screw selftap 6.5x20mm 00662406520 Hgp ii acetabular cup bone screw selftap 6.5x25mm 006624
  • Z-1110-2016 · Jan 11, 2016 · Terminated
    Product 12 consists of all product under product code JDI , and same usage: Item no: 902602935 6 DEGREE COCR FEM HEAD 28 902602835 6 DEGREE COCR FEM HEAD 28 902603235 6 DEGREE COC
  • Z-0849-2016 · Jan 11, 2016 · Terminated
    VERSYS 6 INCH BEADED FC 1 VERSYS 6 INCH BEADED FC S VERSYS 8 INCH BEADED FC 1 VERSYS 8 INCH BEADED FC 2 prosthesis, hip, semi-constrained, metal/polymer, porous uncemented "" Tota
  • Z-1131-2016 · Jan 11, 2016 · Terminated
    Product 33 consists of all product under product code: JDI and same usage: Item no: 662406515 HGP II ACETABULAR CUP BON 662406520 HGP II ACETABULAR CUP BON 662406525 HGP II ACETA
  • Z-1126-2016 · Jan 11, 2016 · Terminated
    Product 28 consists of all product under product code: JDI and same usage: Item no: 32902605000 FEMORAL HD 28MM MEDIUM 32902604000 FEMORAL HD 28MM SHORT 32902604035 FEMORAL HD 28M
  • Z-1127-2016 · Jan 11, 2016 · Terminated
    Product 29 consists of all product under product code: LPHand same usage: Item no: 32902603800 FEMORAL HEAD +0.5 X 22 MM 32902604810 FEMORAL HEAD +3.5 X 22 MM 32902604845 FEMORAL
  • Z-1137-2016 · Jan 11, 2016 · Terminated
    Product 39 consists of all product under product code: JDI and same usage: Item no: 32902605800 ION IMPLANTED FEM 22MM LO 32902604900 ION IMPLANTED FEM 26MM ME 32902603900 ION IM
  • Z-1033-2014 · Oct 11, 2013 · Terminated
    6 DEGREE COCR FEM HEAD (various sizes) and 6 DEG UNIPOLAR FEMORAL HE
  • Z-1036-2014 · Oct 11, 2013 · Terminated
    CPT DEGREE TAPER (various sizes) and FEMORAL HD (various sizes)

…and 8 more.

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

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Sources and updates

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