Smith & Nephew Issues Nationwide Recall of RF Denervation Probes Used for the Spine

Source | FDA

FOR IMMEDIATE RELEASE — Andover, MA — March 26, 2007 — Smith & Nephew Inc. is initiating a nationwide recall of 539 RF Denervation probes for the part numbers and models listed in the table below.

The Smith & Nephew RF Denervation probes are indicated for use exclusively with the Smith & Nephew ELECTROTHERMAL(TM) 20S SPINE SYSTEM in RF heat lesion procedures for the relief of pain. The RF Denervation Probes, which are provided in a non-sterile condition, were mislabeled as sterile which potentially could result in a patient infection.

Customers who have product that is being recalled should return it to Smith & Nephew per the recall instructions. The recall includes the following products and lot numbers:

Part #

Description

Lot numbers

7210270

RF Denervation Probe

602549, 602550, 602846, 602847

7210271

RF Denervation Probe

602541, 602542, 602556, 602557, 602558, 602559, 602560, 602561, 602562, 602848, 602849, 602999

7210272

RF Denervation Probe

602543, 602570, 602571, 602850, 603000

The company voluntarily recalled the products after learning of the labeling error. FDA has been apprised of this action. No injuries have been reported to date associated with this issue.

Product was distributed to 134 domestic and international customers. It can be identified by the product number, name, and lot numbers identified above. Smith & Nephew has notified its distributors and customers and is arranging for return and replacement of all recalled products.

Denervation Probe Investigation

If you or a loved one have used the Smith & Nephew probe and received a serious infection; we would like to speak with you. Please contact us by using the form at the bottom of this page or by dialing (866) 588-0600.