Home / Recalls / Vilex In Tennessee Inc / Z-1722-2015

Z-1722-2015 Class II Terminated

Recalled by Vilex In Tennessee Inc — Mcminnville, TN

Recall Details

Product Type
Devices
Report Date
June 17, 2015
Initiation Date
April 22, 2015
Termination Date
October 30, 2016
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
7 units

Product Description

Vilex, Inc., FUZE 10.0 mm x 200 mm, Product # FZ100-200T-25. Ankle arthrodesis, tibio-talo-calcaneal arthrodesis.

Reason for Recall

Incidence of breakage is higher than expected.

Distribution Pattern

Distributed in the states of MS, MD, PA, and TX.

Code Information

all codes

Other recalls by Vilex In Tennessee Inc

  • Z-1721-2015 Class II — Vilex, Inc., FUZE 10.0 mm x 150 mm, Product # FZ100-150T-25. Ankle arthrodesi (April 22, 2015)
  • Z-1723-2015 Class II — Vilex, Inc., FUZE 10.0 mm x 250 mm, Product # FZ100-250T-25. Ankle arthrodesi (April 22, 2015)