Wright Medical recalls Charlotte MTP Hex Screw Model 411: Incorrect product in packaging. Affected units sold with specific lot numbers. Contact for replacement.
Incorrect product is contained in the packaging.
Wright Medical is recalling a specific screw component due to incorrect product being packaged. This could lead to improper use in medical procedures if the wrong screw is installed.
The packaging contains the wrong screw model, which could be installed incorrectly during surgery. This might cause improper fixation of the foot, potentially leading to complications.
Medical professionals using the Charlotte MTP Hex Screw component in Lisfranc Reconstruction Systems. Patients receiving this component during surgery are at risk if the wrong screw is used.
Check for model #41122718, 2.7mm x 18mm, with lot numbers 02010697711582590 or 02010697711582591. The screw is part of the Charlotte Lisfranc Reconstruction System.
Verify the model number and lot numbers to confirm if your screw is affected.
The recall is due to incorrect packaging, not inherent danger. If used correctly, the product is safe.
Look for model #41122718, 2.7mm x 18mm, with lot numbers 02010697711582590 or 02010697711582591.
The recall does not specify a remedy, so contact Wright Medical for guidance.
We’ve drafted a message you can send Wright Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0401-2022 — Wright Medical Wright Medical Hello, I own a Wright Medical that is covered by recall Z-0401-2022 from Wright 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.
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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.
