Skip to content

NA 6624-65-25Recalls & reported problems

Zimmer, Inc. · Class 2

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

Adverse event reports
2
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024127654), received between Feb 24, 2020 and May 26, 2021 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Loosening of Implant Not Related to Bone-Ingrowth” (1 report).

9 other recalls cover devices cleared under the same FDA submission (K840643, K921308); 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

  • Loosening of Implant Not Related to Bone-Ingrowth1
  • Packaging Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • Rheumatoid Arthritis1

Recent adverse event reports

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

  • MalfunctionMay 26, 2021Packaging Problem; Packaging Problem

    IT WAS REPORTED THAT THE STERILE PACKAGE WAS DAMAGED. NO ADVERSE EVENTS HAVE BEEN REPORTED AS A RESULT OF THE MALFUNCTION. ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11884881 ↗
  • InjuryFeb 24, 2020Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth

    IT WAS REPORTED THAT APPROXIMATELY 17 MONTHS POST IMPLANTATION, THE PATIENT WAS REVISED DUE TO LOOSENING OF THE ACETABULAR COMPONENTS. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

    Patient problems: Rheumatoid Arthritis

    MAUDE report 9746153 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K840643, K921308. One submission often covers many models, so check the product and lot details in each record.

  • 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-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-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-1026-2014 · Oct 11, 2013 · Terminated
    HGP II ACETABULAR CUP MOD
  • Z-1036-2014 · Oct 11, 2013 · Terminated
    CPT DEGREE TAPER (various sizes) and FEMORAL HD (various sizes)
  • Z-1025-2014 · Oct 11, 2013 · Terminated
    HGP II ACETABULAR CUP BON

Other PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices

All PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices →

Sources and updates

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