Device recall

Z-1559-2014: Bard Fixt Suture Braided Polyester, Rx Only, Teleflex Medical, Research Triangle…

FDA device recall · Class II · Teleflex Medical

Key facts

Recall number (Z-number) Z-1559-2014
Recall event 67711
Product Bard Fixt Suture Braided Polyester, Rx Only, Teleflex Medical, Research Triangle Park, NC USA Assembled in Mexico. Indicated for use in soft tissue approximation.
Product code GAT
Recalling firm Teleflex Medical
Recall class Class II
Status Terminated
Termination date Aug 14, 2017
510(k) numbers K063778, K930738
FEI number 3005747797

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

Browse all FDA device recalls (products)