Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Smith & Nephew 5.5 mm Dyonics Bonecutter Recalled by Smith & Nephew, Inc. Endoscopy Division Due to Device labeled with an expiry period of 48...
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. Endoscopy Division directly.
Affected Products
Smith & Nephew 5.5 mm Dyonics Bonecutter ,Electroblade Full Radius Part Number: 7205962 Product Usage: The Dyonics Electroblade Resector is indicated for use in arthroscopic surgical procedures of large and small articular cavities. The Dyonics Electroblade Resector is effective in soft and osseous tissue resection and in hemostasis of bleeding vessels. It is intended for arthroscopic procedures using saline solution, Ringers lactate or other conductive solutions as an irrigant under direct or video assisted fiberoptic visualization.
Quantity: 108 units
Why Was This Recalled?
Device labeled with an expiry period of 48 months instead of 36 months; an additional 12 months for which product and package reliability has not been validated.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Smith & Nephew, Inc. Endoscopy Division
Smith & Nephew, Inc. Endoscopy Division has 37 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report