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FDAApril 13, 2022device

AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe

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

The hazard

Product labeled incorrectly.

What to do

FDA enforcement status: Terminated

Brands named

northgate technologiesnorthgate

UPCs

00817183020448

Recall history

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

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AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe — Recall Details · AllClear