Reported Apr 23, 2025 · Ongoing

restor3d Cordera Hip System. ACETABULAR LINER GRP C 36MM LIP. Model Number: HDL-060-C22L-000101 Acetabular Liner for…

Conformis Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Conformis Inc. · 600 Research Dr · Wilmington, MA · 01887-4437

Is this the product you have?

  • restor3d Cordera Hip System. ACETABULAR LINER GRP C 36MM LIP
  • Model NumberHDL-060-C22L-000101 Acetabular Liner for Cordera Hip System
Lot codes and dates
  • Model NumberHDL-060-C22L-000101
  • UDI-DIM572HDL060C22L011
  • Lot1788258
Amount recalled
16

Where it was sold

Why it was recalled

The hip cup liner that was packaged with the incorrect labeling. HDL-060-C22S-000101 from Lot 1788258 contained a hooded liner, but it was labeled to have a standard liner.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Conformis Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:58 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.