Zimmer Biomet recalls Biomet Oxford Partial Knee Phase 3 drill guides with lot number ZB110301 due to potential corrosion from incorrect raw materials. Affected users should contact for details.
Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.
Zimmer Biomet is recalling certain partial knee drill guides that may corrode due to incorrect raw materials. This could lead to complications during surgery if the drill guide fails.
The drill guide may corrode because of incorrect raw materials used by the supplier. This corrosion could cause the drill guide to fail during surgery, potentially leading to complications.
Surgical patients and medical professionals using the specific drill guides with lot number ZB110301. Patients undergoing knee surgery are most at risk if the drill guide fails during procedure.
Check for the item number 32-420324 and lot number ZB110301 on the drill guide. This product was sold as part of Biomet Oxford Partial Knee Phase 3 surgery kits.
Reach out to Zimmer Biomet for specific instructions on how to handle the recalled drill guide.
The recall states there is a potential for corrosion due to incorrect raw materials, which could lead to complications during surgery if the drill guide fails.
Contact Zimmer Biomet directly for specific instructions on handling the recalled drill guide.
Look for item number 32-420324 and lot number ZB110301 on the drill guide. This product was sold as part of Biomet Oxford Partial Knee Phase 3 surgery kits.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-1739-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-1739-2019 from Zimmer Biomet. 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.
