Recall Z-1624-2015— Wright Medical Technology, Inc.

Name: FDA recall Z-1624-2015
Creator: U.S. Food and Drug Administration
Published: 2015-04-16

Class II · Terminated

Class II FDA medical device recall by Wright Medical Technology, Inc., initiated 2015-04-16, terminated 2018-10-18. FDA's recall record names no specific 510(k) clearance for this event. Product: PHALINX (TM) HAMMERTOE HANDLE, SIZE: X-SMALL, STYLE: ANGLED, REF 45304011, CONTENTS 1 EACH, RX ONLY. Reason: The term DORSAL was laser etched on the incorrect side on some of the angled handles..

Recalling firm: Wright Medical Technology, Inc.
Classification: Class II
Status: Terminated
Initiated: 2015-04-16
Terminated: 2018-10-18
Firm location: Memphis, TN, United States

Product description

PHALINX (TM) HAMMERTOE HANDLE, SIZE: X-SMALL, STYLE: ANGLED, REF 45304011, CONTENTS 1 EACH, RX ONLY

Reason for recall

The term DORSAL was laser etched on the incorrect side on some of the angled handles.

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