Smith & Nephew, Inc. INTEGRA SURFIX ALPHA Screwdriver Torx 10, REF 219 135 ND Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
INTEGRA SURFIX ALPHA Screwdriver Torx 10, REF 219 135 ND
Brand
Smith & Nephew, Inc.
Lot Codes / Batch Numbers
UDI: (01)10381780052234 (11)21101 (10)FVRG, Batch Numbers: FTL9, FTLA, and FVRG
Products Sold
UDI: (01)10381780052234 (11)21101 (10)FVRG, Batch Numbers: FTL9, FTLA, and FVRG
Smith & Nephew, Inc. is recalling INTEGRA SURFIX ALPHA Screwdriver Torx 10, REF 219 135 ND due to The affected screwdrivers are out of specification and may not mate with the Surfix Alpha Lock screw. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The affected screwdrivers are out of specification and may not mate with the Surfix Alpha Lock screw
Recommended Action
Per FDA guidance
The firm initiated the recall by letter and email on 01/04/2022. The letter requested that the consignee examine their inventory, quarantine all affected units, and return the completed response form. Entities who have further distributed the product were directed to notify their customers. The firm is seeking return of the product.
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