Recall Z-0567-2020— Wright Medical Technology, Inc.

Class II · Terminated

Class II FDA medical device recall by Wright Medical Technology, Inc., initiated 2016-11-08, terminated 2020-11-03. FDA's recall record names no specific 510(k) clearance for this event. Product: Dart Fire HEADED SCREW 4.0X 32MM, Part Number D1S40032S. 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

Product description

Dart Fire HEADED SCREW 4.0X 32MM, Part Number D1S40032S

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.