Wright Medical recalls Ortholoc 3Di Fusion plates with incorrect dorsiflexion laser markings. This could lead to improper bone alignment during surgery. Affected units have specific lot numbers.
Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts.
Wright Medical is recalling certain Ortholoc 3Di Fusion plates that have incorrect laser markings for dorsiflexion. This could cause improper bone alignment during surgery if used without correction.
The laser markings on the plates indicate incorrect dorsiflexion angles. If the surgeon uses these plates without verifying the markings, it could lead to improper bone alignment during surgery. However, this is a manufacturing error rather than a safety hazard.
Surgical patients and medical professionals who received the recalled Ortholoc 3Di Fusion plates with specific lot numbers. The risk is low as the issue relates to laser marking accuracy, not immediate safety hazards.
Check for the model 'Ortholoc 3Di Fusion Plate MTP Right' with lot number 1736809 or UDI/DI 00889797101011. The product is used for bone stabilization and fixation in surgical procedures.
Verify the lot number and UDI/DI code on the plate to confirm if it matches the recalled units.
The recall is due to incorrect dorsiflexion descriptions laser marked on the plates, which could affect surgical alignment.
Check for the specific lot number 1736809 or UDI/DI code 00889797101011 on the Ortholoc 3Di Fusion Plate MTP Right.
The official recall notice does not specify a remedy or action for affected units.
We’ve drafted a message you can send Wright Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1466-2023 — Wright Medical Wright Medical Hello, I own a Wright Medical that is covered by recall Z-1466-2023 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.
