FDAMay 24, 2017device

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

northgate technologiesnorthgate

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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