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Recap Hip System US157342Recalls & reported problems

Biomet Orthopedics, LLC · Class 2 · Implant

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

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier.

2 other recalls cover devices cleared under the same FDA submission (K071053, K992367); 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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Aug 21, 2019Terminated

    Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.

    Z-0523-2020 · Root cause: Environmental control · FDA record ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K071053, K992367. One submission often covers many models, so check the product and lot details in each record.

  • Z-0528-2020 · Aug 21, 2019 · Terminated
    HA Pins (DFS HA Cort Screw), Hoffman/Colles Pins (Colles CSER Sterile w/ Pin Kit) Item Nos: HAA60-09030 HAA60-09040 HAA60-10030 HAA60-10040 HAA60-11030 HAA60-11040 HAA60-11050 HAA
  • Z-1823-2016 · Apr 1, 2016 · Terminated
    Various trauma and sports medicine instruments and implants. Screw, fixation, bone.

Other Prosthesis, hip, femoral, resurfacing devices

All Prosthesis, hip, femoral, resurfacing devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.