FDA Medical devices recall ·
CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver recall
- Recall number
- Z-3018-2026
- Date
- (initiated July 14, 2026)
- Company / brand
- ConMed Corporation
525 French Rd, Utica, NY, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 2 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESYs CrossFT Suture Anchor with two, #2 (5 metric) Hi-Fi Sutures Sterile
Why was it recalled?
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI:10845854042472, Lot number 1513167
Distribution
US Nationwide distribution in the state of TX.
States: Texas
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-3018-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.