Reported Jun 15, 2022 · Terminated

AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe

Northgate Technologies, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Northgate Technologies, Inc. · 1591 Scottsdale Ct · Elgin, IL · 60123-9361

Is this the product you have?

  • AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe
Lot codes and dates
  • NTI Catalog Number 72-00322-0 / BSC Catalog No. M00546620
  • Lot codeBSC15876
  • GTIN00817183020448
Amount recalled
55 probes

Where it was sold

  • Nationwide
  • MA

Why it was recalled

Product labeled incorrectly.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Nov 8, 2022 · Data as of Sep 19, 6:55 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.