Synthes recalls MatrixNEURO 5mm screws with incorrect 4mm labeling on one lot (30P6198) that could lead to improper bone fixation during surgery.
One lot of MatrixNEURO 5mm screws was packaged in a body clip etched "4", which indicated a 4mm screw. The outer package labeling correctly identifies a 5mm screw, but the body clop incorrectly identifies a shorter length for the screw.
Synthes recalls a specific lot of MatrixNEURO 5mm screws that were incorrectly labeled as 4mm. This could cause improper bone fixation during cranial or facial surgery if used without correction.
The screws are labeled as 4mm but are actually 5mm. Using them in procedures requiring precise bone fixation could lead to improper healing or complications.
Surgical teams using the recalled lot (30P6198) for cranial or facial procedures. Patients undergoing surgery with these screws are at risk of improper fixation.
Check for the lot number 30P6198 on the outer packaging. The screws are intended for cranial bone and facial fixation in surgeries like craniotomies.
Look for the lot number 30P6198 on the outer packaging of the MatrixNEURO screws.
The recalled lot number is 30P6198.
The screws were incorrectly labeled as 4mm but are actually 5mm, which could affect bone fixation during surgery.
The official recall notice does not specify a remedy or action steps beyond checking the lot number.
We’ve drafted a message you can send Synthes to request your refund or repair — edit it as you like.
Subject: Recall Z-2698-2020 — Synthes Synthes Hello, I own a Synthes that is covered by recall Z-2698-2020 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.
