FDAFDA · Food and drugs·Recall number Z-1619-2013
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. Reattachment of soft tissue to bone in orthopedic surgical procedures
Published July 10, 2013 · Recall initiated: March 6, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Incorrect blue/white suture was used.
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- Linvatec Corp. dba ConMed Linvatec
- Distributor
- US Distribution including the states of FL, KY, LA, MI, NC, and NY.
- Lot
- Product Number CFBC-4502, Lot #431437
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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