Linvatec Corp. dba ConMed Linvatec: Medical Device Recall in 2013 - (Recall #: Z-1619-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: March 6, 2013

Date Posted: July 10, 2013

Recall Number: Z-1619-2013

Event ID: 65166

Reason for Recall:

Incorrect blue/white suture was used.

Status: Terminated

Product Quantity: 60 each of both units

Code Information:

Product Number CFBC-4502, Lot #431437

Distribution Pattern:

US Distribution including the states of FL, KY, LA, MI, NC, and NY.

Voluntary or Mandated:

Voluntary: Firm initiated