FDA recall record

Northgate Technologies Electrohydraulic lithotripter probe, 1.9 FR 375 cm, Model 9-195-371DS recall — FDA Z-0073-2018

The inner and outer labels on the product contain incorrect reference number of 9-202-3751DS. According to Northgate Technologies, the resistor in the…

Class IIclassification
Z-0073-2018official record ID
Nov 15, 2017report date

Recall record at a glance

Official recordZ-0073-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNorthgate Technologies, Inc.
Report dateNov 15, 2017
Recall initiation dateMay 24, 2017
Quantity186
LocationElgin, IL, United States

Official product description

Electrohydraulic lithotripter probe, 1.9 FR 375 cm, Model 9-195-371DS used with a Model 9-201-00 Autolith lithotripter. electrohydraulic lithotripsy (EHL) is a method that allows large stones to be fragmented and removed percutaneously or endoscopically.

Why the product was recalled

The inner and outer labels on the product contain incorrect reference number of 9-202-3751DS. According to Northgate Technologies, the resistor in the probe will not allow the mislabeled product to be used with the incorrect generator. Could Delay Care.

Distribution information

US Distribution to the following states : MA, NE and TN and Internationally to Canada.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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