GENESYS Cross FT Suture Anchor with Two #2 recall
GENESYS Cross FT Suture Anchor with Two #2 (5 metric) Hi-FI Registered Trade Mark Sutures Rx Only STERILE EO CONMED LINVATEC REF CFBC-4502.…
Why was GENESYS Cross FT Suture Anchor with Two #2 recalled?
Incorrect blue/white suture was used.
What should I do if I have this product?
Review the official FDA enforcement record for current 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?
Product Number CFBC-4502, Lot #431437
- Product
- GENESYS Cross FT Suture Anchor with Two #2 (5 metric) Hi-FI Registered Trade Mark Sutures Rx Only STERILE EO CONMED LINVATEC REF CFBC-4502.…
- Recalling firm
- Linvatec Corp. dba ConMed Linvatec
- Quantity
- 60 each of both units
- Distribution
- US Distribution including the states of FL, KY, LA, MI, NC, and NY.
- Recall date
- July 10, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)