FDA Enforcement Class II Terminated

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 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.

Recall: Z-2144-2012 · Reported August 15, 2012

Enforcement

Recall Number
Z-2144-2012
Event ID
62617
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Smith & Nephew, Inc. Endoscopy Division
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
August 15, 2012
Initiation Date
July 14, 2012
Classification Date
August 3, 2012
Termination Date
March 22, 2021
Address
150 Minuteman Drive, Andover, MA, 01810-1031, United States

Description

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 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.

Reason

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.

Code Info

Lot Numbers: 950135R, 950136R, 950137R, 950138R

Distribution

Worldwide Distribution - US Nationwide and the countries of : Australia, Canada, Korea, Turkey, UAE, and Japan.

Quantity

340 units