- Recalling firm
- Medartis AG
- Reason for recall
- The cannulation of the CCS screw is not centered.
- Affected products (lot / model / serial)
- UDI/DI 07630037887706, Lot Numbers: 25444702, 24425542, 24404471, 25441997
- Units affected
- 13 units
- Distribution pattern
- US Nationwide distribution in the states of LA, TX. IN, CA, NC.
- Firm location
- Basel Town, N/A, Switzerland
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- E-Mail
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2361-2026
- Recall initiated
- April 24, 2026
- FDA classification date
- June 9, 2026
- FDA report date
- June 17, 2026
- FDA event ID
- 98952
- Last updated on HTM Vibe
- July 23, 2026