FDAClass IIJune 17, 2026

Medartis APTUS recall

Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation

Why was Medartis APTUS recalled?

The cannulation of the CCS screw is not centered.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI/DI 07630037887706, Lot Numbers: 25444702, 24425542, 24404471, 25441997

Product
Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation
Recalling firm
Medartis AG
Quantity
13 units
Distribution
US Nationwide distribution in the states of LA, TX. IN, CA, NC.
Recall date
June 17, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls