Home / Recalls / Medical Devices
Northgate Technologies, Inc. recalls AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe
Recalled June 15, 2022 · FDA recall Z-1235-2022 · Northgate Technologies
Hazard
Product labeled incorrectly. · FDA Class II
Units
55 probes
Sold at
US Nationwide distribution in the state of MA.
Description
Product labeled incorrectly.
Product
AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe
Manufacturer(s)
Northgate Technologies, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →