APTUS 2.5 TriLock Screw Recall: Mix-up Between 2.5mm and 2.8mm Screws

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Recalling firmMedartis AGHochbergerstrasse 60e, N/A · Basel Town, N/A N/A

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Medartis recalls APTUS 2.5 TriLock Screws (model A-5750.16/1) because they can be mistaken for 2.8mm screws. This mix-up could lead to improper use in hand, foot, or joint repairs. The recall affects specific lots sold in 2023.

Why it’s dangerous

The screws have a small chance of being confused with 2.8mm screws due to similar packaging. Using the wrong size could cause improper fixation in fractures or joint repairs, potentially leading to complications.

Who’s affected

Hand, foot, and joint repair patients using APTUS 2.5 TriLock Screws (model A-5750.16/1) from lot 25472432 are most at risk. Surgeons and medical staff handling these screws may also be affected.

How to tell if you have this one

Check for the model number A-5750.16/1 on the packaging. The lot code 25472432 is specific to this recall. These screws were sold in 2023 for hand, foot, and joint repairs.

Brand
APTUS
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for the model number A-5750.16/1 and lot code 25472432 on the packaging.

✎ GovInfoNow

Questions people ask

Why is this recall happening?

The screws may be confused with 2.8mm screws, which could lead to improper use in hand, foot, or joint repairs.

What is the specific model number for this recall?

The model number is A-5750.16/1.

How can I tell if I have the recalled screws?

Check for the model number A-5750.16/1 and lot code 25472432 on the packaging.

Take action

Contact APTUS

We’ve drafted a message you can send APTUS to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1549-2026 — APTUS APTUS

Hello,

I own a APTUS that is covered by recall Z-1549-2026 from APTUS.

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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Where this comes from

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.

Official source: FDA Recall #Z-1549-2026 (January 9, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1549-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Medartis AG recalls Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version:

Lower-risk recall