CONMED Linvatec GENESYS CrossFT Suture Anchor with recall
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…
Why was CONMED Linvatec GENESYS CrossFT Suture Anchor with recalled?
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI:10845854042472, Lot number 1513167
- 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…
- Recalling firm
- ConMed Corporation
- Quantity
- 2 units
- Distribution
- US Nationwide distribution in the state of TX.
- Recall date
- September 2, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)