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PAR 5 HAP HIP SYSTEMRecalls & reported problems across all models

Biomet Orthopedics, LLC · 5 models in the FDA device registry

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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

We found 5 models of PAR 5 HAP HIP SYSTEM by Biomet Orthopedics, LLC in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

1 FDA recall record name at least one of these models by its device identifier.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

PAR 5 HAP HIP SYSTEM recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

  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 · names 5 of these models · Recall details · FDA record ↗

PAR 5 HAP HIP SYSTEM models

5 models, most reported first. Each model has its own page with its reports, recalls and device details.

Other Biomet Orthopedics, LLC products

All Biomet Orthopedics, LLC devices →

Sources and updates

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