APTUS 2.8 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 AG recalls APTUS 2.8 TriLock Screws (model A-5850.16/1) because they may be mixed up with 2.5mm screws. Using the wrong size could cause improper bone fixation during surgery.

Why it’s dangerous

The screws may have the wrong outer diameter (2.5mm instead of 2.8mm). This could lead to improper bone fixation during surgery, potentially causing complications like misalignment or instability.

Who’s affected

Medical professionals using APTUS 2.8 TriLock Screws (model A-5850.16/1) for hand, foot, shoulder, or forearm procedures. Patients undergoing surgery with these screws are at risk if the wrong size is used.

How to tell if you have this one

Check the lot code on the packaging: 25467933. The product is a 2.8 TriLock Screw 16mm, HD7, 1/Pkg with model number A-5850.16/1.

Brand
APTUS
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Verify the lot code is 25467933 and the model number is A-5850.16/1.

✎ GovInfoNow

Questions people ask

Why is this screw being recalled?

The screws may be mixed up between 2.5mm and 2.8mm outer diameter, which could lead to improper bone fixation during surgery.

What should I do if I have this product?

The recall does not specify a remedy, so check the product details to confirm if it's affected.

Is there a risk of serious injury?

The recall states a mix-up between screw sizes, but no specific injury mechanism is described. This is considered low risk.

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-1550-2026 — APTUS APTUS

Hello,

I own a APTUS that is covered by recall Z-1550-2026 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-1550-2026 (January 9, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1550-2026 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: 2.8 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5850.16/1 Software Version:

Lower-risk recall