Neurotherm, Inc. NeuroTherm Simplicity III RF Electrode Model Number: RFDE-SI The lesioning of neural tissue. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
NeuroTherm Simplicity III RF Electrode Model Number: RFDE-SI The lesioning of neural tissue.
Brand
Neurotherm, Inc.
Lot Codes / Batch Numbers
Lot numbers: 080630- 1 B and 080630- 1 C Exp. June 2011
Products Sold
Lot numbers: 080630- 1 B and 080630- 1 C Exp. June 2011
Neurotherm, Inc. is recalling NeuroTherm Simplicity III RF Electrode Model Number: RFDE-SI The lesioning of neural tissue. due to Distal tip may detach from the probe. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Distal tip may detach from the probe
Recommended Action
Per FDA guidance
NeuroTherrn sales representatives were notified telephonically or through e-mail. End users were notified through visits by NeuroTherm sales representatives on 7/28/08 and 8/15/08. For questions, please contact NeuroTherm, Inc. at 1-978-777-3916.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CO, FL, IL, OH, TN, TX, VA, WY
Page updated: Jan 10, 2026