Medartis AG recalls Medartis APTUS
- Recalling company
- Medartis AG
- Product
- Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation
- Reason
- The cannulation of the CCS screw is not centered.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Apr 24, 2026
- Reported
- Jun 17, 2026
- Distribution
- US Nationwide distribution in the states of LA, TX. IN, CA, NC.
- Status
- Ongoing
- Quantity
- 13 units
- Lot / codes
- UDI/DI 07630037887706, Lot Numbers: 25444702, 24425542, 24404471, 25441997
- Company location
- Basel Town, N/A
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2361-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2361-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.