Medical device recalls Moderate risk

Smith & Nephew, Inc. recalls Smith & Nephew ACUFEX TRUNAV Retrograde Drill 5.5MM Product Number: 72204037 The ACUFEX TRUNAV Retrograde Drill is inte…

Recall date
March 15, 2017
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1838-2017
FDA classification
Class II
Brand / firm
Smith & Nephew, Inc.
Sold / distributed
Worldwide Distribution - US (Nationwide) and Internationally to AU, CL, DB, DE, ES, FR, GB, NL, SE

Why it was recalled

Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Smith & Nephew ACUFEX TRUNAV Retrograde Drill 5.5MM Product Number: 72204037 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone

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