Medartis recalls APTUS cannulated compression screws due to misaligned cannulation, which may cause improper bone fixation. Affected units include specific model and lot numbers.
The cannulation of the CCS screw is not centered.
Medartis is recalling certain cannulated compression screws for bone fixation because the cannulation isn't centered. This could lead to improper bone healing if used in surgery.
The cannulation (the hole for the screw) isn't centered properly. This could cause the screw to not fit correctly in the bone, potentially leading to improper healing or complications during surgery.
Surgical patients who received the recalled screws during procedures. Surgeons and medical facilities using the specific model and lot numbers are most at risk.
Check for the model '5.0 headedCCS Long Thread 50/20mm' and lot numbers 25444702, 24425542, 24404471, or 25441997. The product is labeled with UDI/DI 07630037887706.
Verify the model number and lot numbers listed in the recall notice to confirm if your screws are affected.
The cannulation of the screw is not centered, which could lead to improper bone fixation during surgery.
The recall notice does not specify a remedy; check the product details to see if your screws are affected.
The misaligned cannulation could cause improper bone healing, but the recall indicates low risk as the hazard is not severe in normal use.
We’ve drafted a message you can send Medartis to request your refund or repair — edit it as you like.
Subject: Recall Z-2361-2026 — Medartis Medartis Hello, I own a Medartis that is covered by recall Z-2361-2026 from Medartis. 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.
