Recall Z-1567-2022— Wright Medical Technology, Inc.

Class II · Ongoing

Class II FDA medical device recall by Wright Medical Technology, Inc., initiated 2022-07-27. FDA's recall record names no specific 510(k) clearance for this event. Product: Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.. Reason: An incorrect sizing label was applied to the carton packaging..

Recalling firm
Wright Medical Technology, Inc.
Classification
Class II
Status
Ongoing
Initiated
2022-07-27
Firm location
Memphis, TN, United States

Product description

Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.

Reason for recall

An incorrect sizing label was applied to the carton packaging.

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