Recall Z-0566-2020— Wright Medical Technology, Inc.

Name: FDA recall Z-0566-2020
Creator: U.S. Food and Drug Administration
Published: 2016-11-08

Class II · Terminated

Class II FDA medical device recall by Wright Medical Technology, Inc., initiated 2016-11-08, terminated 2020-11-03. It names one FDA 510(k) clearance: K090857. Product: VALOR SCREW 5.0MM X 45MM LEN, Part Number 4151150045. Reason: The firm discovered a lack of adequate documentation confirming sterility on certain products..

Recalling firm: Wright Medical Technology, Inc.
Classification: Class II
Status: Terminated
Initiated: 2016-11-08
Terminated: 2020-11-03
Firm location: Arlington, TN, United States

510(k) clearances named in this recall

1 on FDA's record

K090857 — VALOR ANKLE FUSION NAIL SYSTEMWrightmedicaltechnologyinc·cleared 2009-07-14

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

VALOR SCREW 5.0MM X 45MM LEN, Part Number 4151150045

Reason for recall

The firm discovered a lack of adequate documentation confirming sterility on certain products.

Data sourced from openFDA. This site is unofficial and independent of the FDA.