Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2144-2012 — Smith & Nephew Dyonics Electroblade Resector, 4.5mm Full Radius Blade, BONECUTTER Part Number: 72202213 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

U.S. FDA — Device Enforcement · United States · 2012-07-14 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2144-2012
Date of alert: 2012-07-14
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Smith & Nephew, Inc. Endoscopy Division
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 72202213

Reported risk: Devices 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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