Device recall

Z-0662-2007: RF Denervation Probe, 5cm, temperature sensing electrodes designed for use in…

FDA device recall · Class I · Smith & Nephew, Inc. Endoscopy Division

Key facts

Recall number (Z-number) Z-0662-2007
Recall event 37232
Product RF Denervation Probe, 5cm, temperature sensing electrodes designed for use in radiofrequency lesion procedures for the treatment of pain. Part Number: 7210270
Product code GXI
Recalling firm Smith & Nephew, Inc. Endoscopy Division
Recall class Class I
Status Terminated
Termination date Jan 18, 2008
510(k) numbers K034012
FEI number 3003604053

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

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