AVID Medical recalls Halyard Total Knee Kits (Model ESJH012-07) due to potential metal flakes causing surgical site reactions. Affected kits sold from 2016-06-09.
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing local reactions or possible foreign body reactions
AVID Medical is recalling Halyard Total Knee Kits (Model ESJ: ESJH012-07) because metal flakes could detach and enter surgical sites, causing reactions. This is a serious risk for patients undergoing knee surgery.
Small metal flakes from the sponge forceps and towel clamps may detach during surgery. If these flakes enter the surgical site, they could cause local reactions or foreign body reactions in the patient.
Patients who received the recalled Halyard Total Knee Kits (Model ESJH012-07) during surgery are most at risk. Healthcare providers using these kits for procedures are also affected.
Check for the model number ESJH012-07 on the kit packaging. Kits were sold starting June 9, 2016, with lot number 1606092.
Immediately stop using the recalled Halyard Total Knee Kits (Model ESJH012-07) as metal flakes could cause surgical site reactions.
The model number is ESJH012-07.
These kits were sold starting June 9, 2016.
Check the model number on the kit packaging; the recalled model is ESJH012-07 with lot number 1606092.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0390-2025 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-0390-2025 from AVID 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.