FDA recall Z-2361-2026

Medartis AG · Class II · device

Product

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

Reason for recall

The cannulation of the CCS screw is not centered.

Distribution

US Nationwide distribution in the states of LA, TX. IN, CA, NC.

Key facts

Status
Ongoing
Initiation date
2026-04-24
Report date
2026-06-17
Voluntary/Mandated
Voluntary: Firm initiated
Location
Basel Town, N/A, Switzerland

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2361-2026