Reported Jul 30, 2025 · Ongoing

Brand Name: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD42…

Encore Medical, LP

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: Encore Medical, LP · 9800 Metric Blvd · Austin, TX · 78758-5445

Is this the product you have?

  • Brand NameEMPOWR Dual Mobility"
  • Product NameEMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28
  • OD42 Model/Catalog Number952-28-42F
  • Software VersionNA
  • Product DescriptionThe EMPOWR Dual Mobility" system is compatible with the EMPOWR Acetabular¿ system, 28mm femoral
  • heads and all hip stems ComponentNA
Lot codes and dates
  • Lot CodeItem: 952-28-42F
  • GTIN00190446673200
  • Lot2225A1124
Amount recalled
20 units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

Why it was recalled

Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. Issued discovered via a customer complaint.

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

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:02 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.