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BIOMET HIP SYSTEM 163665Recalls & reported problems

Biomet Orthopedics, LLC · Class 2 · Implant

All models of Biomet Hip System (37)

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 05019279400751), received between Jun 9, 2020 and Jun 9, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).

13 other recalls cover devices cleared under the same FDA submission (K911684, K942479, K953925, K974558); 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 Dislocated1

Patient problems

  • Joint Dislocation1

Recent adverse event reports

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

  • InjuryJun 9, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated

    NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

    Patient problems: Joint Dislocation

    MAUDE report 10132812 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K911684, K942479, K953925, K974558. One submission often covers many models, so check the product and lot details in each record.

  • Z-1537-2018 · Apr 2, 2018 · Terminated
    Modular Head Component, Biomet Hip System; Item No. 163669, Hip Joint, metal/polymer semi-constrained cemented prosthesis The device is used in treatment of patients who need tot
  • Z-0650-2016 · Nov 17, 2015 · Terminated
    Biomet Integral Centralizer Hip System, Lateralized Femoral Stem (Co-Cr-Mo), 9mm, 11mm, 13mm, 15mm, and 17mm
  • Z-1757-2015 · Apr 16, 2015 · Terminated
    Biomet Cobalt-Chrome Femoral Components, 32MM MOD HEAD COCR -6MM NECK; 32MM MOD HEAD COCR -3 MM NECK; 32MM MOD HEAD COCR STD NECK ; 32MM MOD HEAD COCR +3MM NECK; 32MM COCR MOD HD
  • Z-1286-03 · Jun 18, 2003 · Terminated
    Stanmore modular hip system; Stanmore CoCr femoral size 1 straight stem; part 164251
  • Z-1284-03 · Jun 18, 2003 · Terminated
    Stanmore modular hip system; Stanmore CoCr femoral size 4 std. stem; part 164244
  • Z-1285-03 · Jun 18, 2003 · Terminated
    Stanmore modular hip system; Stanmore CoCr femoral size 5 std. stem; part 164245
  • Z-1283-03 · Jun 18, 2003 · Terminated
    Stanmore modular hip system; Stanmore CoCr femoral size 3 std. stem; part 164243
  • Z-1287-03 · Jun 18, 2003 · Terminated
    Stanmore modular hip system; Stanmore CoCr femoral size 2 straight stem; part 164252
  • Z-1288-03 · Jun 18, 2003 · Terminated
    Stanmore modular hip system; Stanmore CoCr femoral size 3 straight stem; part 164253
  • Z-1290-03 · Jun 18, 2003 · Terminated
    Stanmore modular hip system; Stanmore CoCr femoral size 5 straight stem; part 164255
  • Z-1281-03 · Jun 18, 2003 · Terminated
    Stanmore modular hip system; Stanmore CoCr femoral size 1 std. stem; part 164241
  • Z-1282-03 · Jun 18, 2003 · Terminated
    Stanmore modular hip system; Stanmore CoCr femoral size 2 std. stem; part 164242
  • Z-1289-03 · Jun 18, 2003 · Terminated
    Stanmore modular hip system; Stanmore CoCr femoral size 4 straight stem; part 164254

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