FDAJuly 14, 2026
ConMed GENESYS CrossFT Suture Anchor Recall
FDA published this notice on July 14, 2026 for Texas.
This notice is kept at its address for anyone who saved the link. AreaZine no longer holds the agency's full record for it, so the page shows what AreaZine recorded and links to the agency's own page, the one to read.
What AreaZine recorded
- Agency
- FDA
- Place
- Texas
- Date
- July 14, 2026
- Recall class
- Class II
- Reason given by the agency
- Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
- Distribution
- US Nationwide distribution in the state of TX.
- Official source
- the notice at its source
Official warnings by state, with every type counted since 2008Search notices, places and declaration numbers
Source: FDA.