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.