FDAClass IIMarch 30, 2016

Neurotherm Curved Radiofrequency recall

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…

Why was Neurotherm Curved Radiofrequency recalled?

Straight needle labeled as a curved needle

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot number: 12131-1C

Product
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…
Recalling firm
Neurotherm, Inc.
Quantity
135 cannulas (27 boxes/5)
Distribution
US Nationwide Distribution in the states of CA ,CO, OH, OR
Recall date
March 30, 2016
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls