Encore Medical, LP recalls EMPOWR Acetabular System: Liner

942-01-40G acetabular system package was found to contain 942-01-36H acetabular system; and several other acetabular system and knee insert devices may also have a packaging discrepancy, which may cause surgical delay to exchange devices or revision surgery.

On 1/5/2026, recall notices were emailed to customers who were asked 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) Contact the firm to arrange for affected device return. 3. Complete and return the acknowledgement and response form via email to Lesli.Helmick@enovis.com Customers with questions can email the firm at productsafety@enovis.com

• FDA enforcement recordOfficial FDA database entry for Z-1234-2026
• FDA 510(k) clearance · K190057The device's official FDA premarket clearance record
• FDA device classification · LPHOfficial FDA classification for this device type
• CFR regulation · 21 CFR 888.3358The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find Encore Medical, LPSearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.