Smith & Nephew, Inc. 6.5MMX165MM CANNULATED SCREW Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
6.5MMX165MM CANNULATED SCREW
Brand
Smith & Nephew, Inc.
Lot Codes / Batch Numbers
Model 71106365S, Lot 20GT39417
Products Sold
Model 71106365S; Lot 20GT39417
Smith & Nephew, Inc. is recalling 6.5MMX165MM CANNULATED SCREW due to The product label incorrectly indicated that the screws are fully threaded, but the screws contained in the package were partially threaded.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The product label incorrectly indicated that the screws are fully threaded, but the screws contained in the package were partially threaded.
Recommended Action
Per FDA guidance
Smith & Nephew issued a customer letter via email dated September 20, 2021. Consignees are asked to inspect inventory and locate any devices from the listed product and batch numbers enclosed with the Urgent Medical Device Recall Notice, and quarantine them immediately. Consignees must complete the enclosed response form, sign and send to FieldActions@smith-nephew.com. Response form shall be completed even if there is no impacted product on hand.
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 noticePage updated: Jan 10, 2026