Recall company profile

Neurotherm, Inc. Recalls

Overview of recall records associated with Neurotherm, Inc., including dates, categories and classifications where available.

1recall records
Apr 20, 2016latest record date
Apr 20, 2016earliest record date

Recall history in this database

Classification mix: Class II: 1.

Medical DeviceApr 20, 2016

Neurotherm NT2000iX RF Generator recall — FDA Z-1361-2016

NT2000iX software shipped with the international setting turned on. The international settings include access to Corodotomy, Bi-Polar, and No Temperature modes were not cleared in the…

Class IIFDA: TerminatedNeurotherm, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Neurotherm, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.