Vilex In Tennessee Inc: Medical Device Recall in 2015 - (Recall #: Z-1722-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: April 22, 2015

Date Posted: June 17, 2015

Recall Number: Z-1722-2015

Event ID: 71344

Reason for Recall:

Incidence of breakage is higher than expected.

Status: Terminated

Product Quantity: 7 units

Code Information:

all codes

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated