Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 73407

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
February 26, 2013
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Neurotherm, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

Neurotherm Curved Radiofrequency (RF) cannnula 10 cm 18 gauge, 10 mm active tip Model Number: C-1010-R-18 Product Usage: The device is a radiofrequency needle, used for the application of radiofrequency energy with as intended result, thermo coagulation of nervous tissue in the human body for pain relief. They are designed to be used to treat chronic pain. During nerve ablation, the needle is used in conjunction with a radiofrequency generator, an electrode and grounding pads.

Z-1247-2016
Recall number
Z-1247-2016
Initiated
February 26, 2013
Classification
Class II
Status
Terminated
Recalling firm
Neurotherm, Inc.
Quantity
135 cannulas (27 boxes/5)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Straight needle labeled as a curved needle

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process control

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Straight needle labeled as a curved needle

Code information

Lot number: 12131-1C

Distribution pattern

US Nationwide Distribution in the states of CA ,CO, OH, OR