Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS — Class II medical device recall Z-2701-2026
Ongoing recall by Encore Medical, LP, reported 2026-07-15, distributed in AL, CO, IA, IL, IN, MI, MT, NC…. Due to packaging discrepancy with incorrect product size mixed up.
| Recall number | Z-2701-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Encore Medical, LP, Austin, TX, United States |
| Recall initiated | 2026-02-16 |
| Classified | 2026-07-08 |
| Reported by FDA | 2026-07-15 |
| Distributed | AL, CO, IA, IL, IN, MI, MT, NC, NE, NY, SD, TX, WY |
| Quantity | 8 |
| UPC / GTIN / UDI-DI | 00888912167086 |
| Lot numbers | 135T1060, 145T1067 |
| Model numbers | 341-14-711 |
| Expiration dates | 2026-12-06 |
Product
Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 341-14-711 Product Description: Enovis knee devices are for knee arthroplasty.
Reason for recall
Due to packaging discrepancy with incorrect product size mixed up.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2701-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.