Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Smith & Nephew BEAVER Blade 4.0mm Part Number: 72203307 Orthopedic Recalled by Smith & Nephew, Inc. Due to Blade exhibiting fracture during hip arthroscopy procedures
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Smith & Nephew, Inc. directly.
Affected Products
Smith & Nephew BEAVER Blade 4.0mm Part Number: 72203307 Orthopedic surgical instrument used in hip arthroscopy.
Quantity: 69043 units
Why Was This Recalled?
Blade exhibiting fracture during hip arthroscopy procedures
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Smith & Nephew, Inc.
Smith & Nephew, Inc. has 220 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report