- Recalling firm
- ConMed Corporation
- Reason for recall
- Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
- Affected products (lot / model / serial)
- UDI:10845854042472, Lot number 1513167
- Units affected
- 2 units
- Distribution pattern
- US Nationwide distribution in the state of TX.
- Firm location
- Utica, NY, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- E-Mail
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-3018-2026
- Recall initiated
- July 14, 2026
- FDA classification date
- August 26, 2026
- FDA report date
- September 2, 2026
- FDA event ID
- 99498
- Last updated on HTM Vibe
- September 8, 2026