Encore Medical recalls EMPOWR 3D Knee Tibial Insert (REF: 342-10-705) due to swapped hip/knee parts risking wrong surgery product. Affected units have specific UDI-DI and lot numbers.
Knee insert and acetabular system parts were swapped within inner pack prior to the product being sealed within the tray, which could result in surgeons not having the correct product for the surgery due to different anatomies (Hip vs Knee).
Encore Medical is recalling a specific knee insert product because parts were swapped with hip components during packaging. This could lead to surgeons using the wrong product during surgery due to anatomical differences between hip and knee joints.
The knee insert and hip implant parts were accidentally mixed within the inner packaging before sealing. This means surgeons might receive the wrong product during surgery because hip and knee implants have different anatomical requirements.
Surgeons using the recalled knee insert for procedures are affected. Patients undergoing knee surgery with this specific product model are at risk of receiving the wrong implant.
Check for the product code REF: 342-10-705. The UDI-DI number is 00888912167321 and the lot number is 075T1167. This product expires March 30, 2028.
Verify the UDI-DI number (00888912167321) and lot number (075T1167) on the packaging.
The recall is for potential mislabeling during packaging, not a safety issue with the product itself when used correctly.
Look for the UDI-DI number 00888912167321 and lot number 075T1167 on the packaging.
The recall does not specify a remedy, so no action is required beyond checking product details.
We’ve drafted a message you can send Encore Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0102-2024 — Encore Medical Encore Medical Hello, I own a Encore Medical that is covered by recall Z-0102-2024 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.
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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.
