Wright Medical Technology, Inc. EasyFuse Dynamic Compression System Instrument Pack Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
EasyFuse Dynamic Compression System Instrument Pack
Brand
Wright Medical Technology, Inc.
Lot Codes / Batch Numbers
Model Number FFSP1530
Products Sold
Model Number FFSP1530, UDI: 00889797103565 Lot Codes (Expiration Date): 781853-110321 (11/03/2029) and 780395-112221 (12/03/2029)
Wright Medical Technology, Inc. is recalling EasyFuse Dynamic Compression System Instrument Pack due to The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.
Recommended Action
Per FDA guidance
A recall notice was disseminated to the distributor and sales representatives via email (09-Mar-2022 and 10-Mar-2022) and to the hospitals via mail (10-Mar-2022, FedEx Priority Overnight). The hospital letters were delivered on 11-Mar-2022. Customers were instructed to immediately check all stock areas and/or operating room storage to determine if any devices from the affected product list are at your facility and remove them from their point of use. They are to return the enclosed business reply form by email to confirm receipt of the notification/document product segregation. Upon receipt of the completed business reply form, Stryker will arrange for the return and replacement of the product(s). Effectiveness checks will be performed through the confirmation of the returned/signed acknowledgement form.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
FL, NC, OH, TX
Page updated: Jan 10, 2026