Reported Feb 9, 2022 · Ongoing

INTEGRA SURFIX ALPHA Screwdriver Torx 10, REF 219 135 ND

Smith & Nephew, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Smith & Nephew, Inc. · 1450 E Brooks Rd · Memphis, TN · 38116-1804

Is this the product you have?

    • INTEGRA SURFIX ALPHA Screwdriver Torx 10
    • REF 219 135 ND
Lot codes and dates
  • UDI(01)10381780052234 (11)21101 (10)FVRG
  • Batch NumbersFTL9, FTLA, and FVRG
Amount recalled
8 units (US)

Where it was sold

Why it was recalled

The affected screwdrivers are out of specification and may not mate with the Surfix Alpha Lock screw

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:37 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.