Synthes recalls MatrixMID: 1.8mm emergency screws with a 3mm instead of 12mm clip marking. This mismatch could lead to improper bone fixation during surgery. Affected units include Lot #41P2340.
One lot of MatrixMIDFACE Emergency Screw 1.8mm, self-tapp, L 12mm, in Clip was packaged with a body clip etched with a 3 (representing 3mm) when it should have been packaged with body clip etched with a 12 (representing 12mm).
Synthes is recalling MatrixMIDFACE Screws that were packaged with a 3mm clip marking instead of the correct 12mm marking. This error could cause improper bone fixation during surgery if used incorrectly.
The screws are designed for precise bone fixation in surgeries. If the clip marking is incorrect (3mm instead of 12mm), the screws might not align properly with the intended bone structure, potentially causing misalignment or improper healing.
Surgical teams using MatrixMIDFACE Screws for cranial bone and facial procedures are affected. The risk is highest for surgeons who used the recalled lot during procedures.
Check for the lot number 41P2340 on the packaging. The screws should have a body clip marked with '12' (representing 12mm), not '3' (representing 3mm).
Look for the lot number 41P2340 and verify the body clip marking is '12' instead of '3'.
The screws were packaged with a 3mm clip marking instead of the correct 12mm marking, which could lead to improper bone fixation during surgery.
The correct body clip marking is '12' (representing 12mm), not '3' (representing 3mm).
The recall record does not specify a remedy, so no action is required beyond checking the packaging.
We’ve drafted a message you can send Synthes to request your refund or repair — edit it as you like.
Subject: Recall Z-2739-2020 — Synthes Synthes Hello, I own a Synthes that is covered by recall Z-2739-2020 from Synthes. 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.
