Zimmer Biomet recalls 2.7mm x 20mm crosslock screws with incorrect sizes (18mm instead of 20mm) that could cause improper bone fixation during surgery. Affected items have specific lot numbers.
One lot of product labeled 2.7mm x18mm Lock Screw Square Drive (Lot 029970) contains 20mm locking screws and one lot of product labeled 2.7mm x 20mm Lock Screw Square Drive (Lot 029980) contains 18mm locking screws
Zimmer Biomet is recalling certain crosslock screws that have the wrong size for surgical use. Using these screws could lead to improper bone fixation and potential complications during surgery.
The recalled screws have incorrect sizes: some contain 18mm screws labeled as 20mm, and others contain 20mm screws labeled as 18mm. This mismatch could cause improper bone fixation during surgery, leading to complications.
Surgical teams using Zimmer Biomet crosslock screws for hand, foot, or small bone procedures may be affected. Patients undergoing surgery with these specific screws are at risk of improper bone fixation.
Check for lot numbers 029970 or 029980 on the packaging. The product is labeled as 2.7mm x 18mm or 2.7mm x 20mm crosslock screws for surgical use.
Look for lot numbers 029970 or 029980 on the packaging to identify affected items.
The recall is due to incorrect screw sizes: some lots contain 18mm screws labeled as 20mm, and others contain 20mm screws labeled as 18mm, which could cause improper bone fixation during surgery.
Check the lot number on the packaging. If it's 029970 or 029980, contact Zimmer Biomet for guidance on next steps.
Yes, using the incorrect screw sizes could lead to improper bone fixation and potential complications during surgery.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0708-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0708-2019 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.
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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.
