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Open, Classified

EMPOWR 3D Knee Tibial Insert, 6R 10MM, VE, REF: 342-10-706

FDA Recall Z-0761-2025 · Posted 2024-12-23

Recalling FirmEncore Medical, LP
Recall StatusOpen, Classified
Product CodeJWH
Date Initiated2024-12-10
Product Quantity9

Reason for Recall

Knee insert package may contain an acetabular system, which may cause surgical delay to get a new product.

Firm Action

On 12/10/2024, recall notices were emailed to customers asking them to do the following: 1. This notice needs to be passed on to all those within your organization or to any organization where the product has been transferred. 2. Review your stock for the products and lot numbers for the items to be returned. 3. Return all devices (quantities listed above) using the RMA number and shipping label provided by Customer Service. 4. Complete and return the acknowledgement and response form via email to [email protected] If you have questions contact the firm at [email protected]

Root Cause

Labeling Change Control

Distribution Pattern

US Nationwide distribution in the states of IN, KS, CA, FL, NY, TX, AL, WA.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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