# FDA recall Z-2361-2026

> **Medartis AG** · Class II · device recall initiated 2026-04-24.

## 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

- **Recall number:** Z-2361-2026
- **Recalling firm:** Medartis AG
- **Classification:** Class II
- **Product type:** device
- **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

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

## Citation

> MORVS. FDA recall Z-2361-2026. Retrieved 2026-10-18 from https://api.morvs.ai/recall/Z-2361-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*