Encore Medical recalls EMPOWR 3D KNEE TIBIAL INSERT E-PLUS model 341-10-711 due to packaging error that may cause incorrect product selection and revision surgery.
Due to packaging discrepancy with the incorrect tibial inserts/implants being packaged. The use of this product may result in the incorrect product being selected. This could result in a revision surgery if used.
Encore Medical is recalling EMPOWR 3D KNEE TIBIAL INSERT E-PLUS model 341-10-711 because packaging errors could lead to the wrong product being selected. This might require revision surgery if used incorrectly.
The packaging discrepancy means the wrong tibial insert might be packaged with the product. Using this incorrect product could lead to a revision surgery being necessary.
Patients who received this specific knee implant model are affected. Those with the model number 341-10-711 are most at risk of needing revision surgery.
Check for the model number 341-10-711 on the packaging. The product was sold with lot code 071T1084.
Verify the model number on the packaging to confirm it is 341-10-711.
The recall is due to packaging discrepancies that could result in the incorrect tibial insert being selected, potentially requiring revision surgery.
Check for model number 341-10-711 on the packaging.
The recall does not specify a remedy, so no action is required unless you suspect the wrong product was selected.
We’ve drafted a message you can send Encore Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2125-2025 — Encore Medical Encore Medical Hello, I own a Encore Medical that is covered by recall Z-2125-2025 from Encore Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.