DePuy Orthopaedics recalls TRUMATCH CT Cut Guide FEM L patient-specific surgical instruments due to a software error that may cause hip, knee, and ankle misalignment during joint replacement surgery. Affected units have part number 420917 and lot number 2795810603295384878.
Software: A coding error associated with the Fast3D Segmentation software. During the scanning process the three images required of the hip, knee and ankle may not be aligned, causing the anatomic landmark locations to potentially result in limb malalignment.
DeP:uy Orthopaedics is recalling TRUMATCH CT Cut Guide FEM L surgical instruments because a software error during scanning could cause limb misalignment during hip, knee, or ankle replacements. This risks improper joint positioning and potential complications after surgery.
A coding error in the Fast3D Segmentation software causes the hip, knee, and ankle images to misalign during the scanning process. This misalignment can lead to incorrect bone marking and improper joint positioning during surgery, potentially causing complications.
Surgical teams using DePuy TRUMATCH CT Cut Guide FEM L instruments for joint replacements are most at risk. Patients who have undergone surgery with these instruments may need follow-up care.
Check for part number 420917 or lot number 2795810603295384878 on the instrument packaging. These instruments were sold as patient-specific surgical tools for joint replacements.
Look for part number 420917 or lot number 2795810603295384878 on the instrument packaging.
A coding error in the Fast3D Segmentation software causes the hip, knee, and ankle images to misalign during the scanning process.
Misaligned images can lead to incorrect bone marking and improper joint positioning, potentially causing complications after surgery.
Check for part number 420917 or lot number 2795810603295384878 on the packaging. If you have the affected model, contact DePuy Orthopaedics for guidance.
We’ve drafted a message you can send DePuy Orthopaedics to request your refund or repair — edit it as you like.
Subject: Recall Z-2400-2021 — DePuy Orthopaedics DePuy Orthopaedics Hello, I own a DePuy Orthopaedics that is covered by recall Z-2400-2021 from DePuy Orthopaedics. 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.
