# FDA recall Z-2147-2025

> **Encore Medical, LP** · Class II · device recall initiated 2025-06-12.

## Product

Brand Name: EMPOWR Dual Mobility"  Product Name: EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40  Model/Catalog Number: 952-28-40E  Software Version: NA  Product Description: The EMPOWR Dual Mobility" system is compatible with the EMPOWR Acetabular¿ system, 28mm femoral heads and all hip stems  Component: NA

## Reason for recall

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

## Distribution

RFK Medical Inc. Viriginia (VA) CE102 952-28-40E 2224A1124A EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40  1  Valor Medical Solutions South Texas (TX)  CE118 952-28-40E 2224A1124A EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40  4 952-28-42F 2225A1124 EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD42  1  Matrix Orthopedics Surgical Devices Dallas/Fort Worth, TX CE120  952-28-40E 2224A1124A EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40  2  WHISKEY TRAIL ORTHOPEDICS LLC   AUS Tennessee (TN)  CE123  952-28-42F 2225A1124 EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD42  1  Florida Direct - FSW Medical Florida (FL) FL001  952-28-40E 2224A1124A EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40  1  Certus Medical LLC Indiana (IN) & Michigan (MI) GL112  952-28-40E 2224A1124A EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD40  1 952-28-42F 2225A1124 EMPOWR Acetabular, Dual Mobility, Poly Bearing, ID28, OD42  1  Procore Med

## Key facts

- **Recall number:** Z-2147-2025
- **Recalling firm:** Encore Medical, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-06-12
- **Report date:** 2025-07-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Austin, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2147-2025

## Citation

> AI Analytics. FDA recall Z-2147-2025. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2147-2025. Source: US FDA. Licensed CC0.

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