FDA Device recall Z-0333-2022

Boston Scientific AUTOLITH TOUCH Bipolar Electrohydraulic Lithotripter, REF M005466800

FDA Device
Class II
ongoing
Published 2021-12-15

On 2021-12-15 the FDA classified a Class II recall of Boston Scientific AUTOLITH TOUCH Bipolar Electrohydraulic Lithotripter, REF M005466800 by Northgate Technologies, citing the languages for Russian, Romanian, Slovak, and Czech have the power settings for high and low switched in the device.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0333-2022
Classification	Class II
Status	ongoing
Initiated	2021-10-25
Published	2021-12-15
Last updated	2026-09-13 11:56 UTC
Company	Northgate Technologies
Distribution	MA

Product

Boston Scientific AUTOLITH TOUCH Bipolar Electrohydraulic Lithotripter, REF M005466800. The device is designed to be used with Northgate Technologies Inc. bipolar disposable EHL probes for the fragmentation of calculi.

Reason

The languages for Russian, Romanian, Slovak, and Czech have the power settings for high and low switched in the device.

Identifiers

code_info	All serial number revisions for the following bracketed base serial numbers distributed between 2/14/2017 and 10/7/2021… All serial number revisions for the following bracketed base serial numbers distributed between 2/14/2017 and 10/7/2021: 21578LAA to 21627LAA 21628BBA to 21662BBA 21667CBA to 21689CBA; 21691CBA to 21697CBA; 21699CBA to 21716CBA 21690CBA, 21698CBA, 21721DBA to 21732DBA; 21734DBA to 21747DBA; 21749DBA to 21756DBA; 21758DBA to 21763DBA; 21765DBA to 21770DBA 21733DBA, 21748DBA, 21757DBA, 21764DBA, 21771EBA to 21781EBA; 21783EBA to 21787EBA; 21789EBA, 21790EBA, 21792EBA to 21800EBA; 21804EBA to 21820EBA 21782EBA, 21788EBA, 21791EBA, 21801EBA to 21803EBA; 21821FBA to 21874FBA 21883HBB to 21942HBB 21954IBB to 22025IBB 22026IBB to 22073IBB 22074IBB to 22130KBB; 22133KBB 22131KBB 22134LBB to 22157LBB 22158ACB to 22229ACB 22230ACB to 22249ACB 22250BCB to 22321BCB 22322CCB to 22393CCB 22394CCB to 22441CCB 22453ECB to 22476ECB 22477FCB to 22488FCB 22489GCB to 22500GCB 22511HCB to 22534HCB 22535ICB to 22558ICB 22559JCB to 22564JCB; 22570JCB to 22575JCB 22566JCB to 22569JCB; 22576JCB, 22577JCB,

code_info

All serial number revisions for the following bracketed base serial numbers distributed between 2/14/2017 and 10/7/2021…

All serial number revisions for the following bracketed base serial numbers distributed between 2/14/2017 and 10/7/2021: 21578LAA to 21627LAA 21628BBA to 21662BBA 21667CBA to 21689CBA; 21691CBA to 21697CBA; 21699CBA to 21716CBA 21690CBA, 21698CBA, 21721DBA to 21732DBA; 21734DBA to 21747DBA; 21749DBA to 21756DBA; 21758DBA to 21763DBA; 21765DBA to 21770DBA 21733DBA, 21748DBA, 21757DBA, 21764DBA, 21771EBA to 21781EBA; 21783EBA to 21787EBA; 21789EBA, 21790EBA, 21792EBA to 21800EBA; 21804EBA to 21820EBA 21782EBA, 21788EBA, 21791EBA, 21801EBA to 21803EBA; 21821FBA to 21874FBA 21883HBB to 21942HBB 21954IBB to 22025IBB 22026IBB to 22073IBB 22074IBB to 22130KBB; 22133KBB 22131KBB 22134LBB to 22157LBB 22158ACB to 22229ACB 22230ACB to 22249ACB 22250BCB to 22321BCB 22322CCB to 22393CCB 22394CCB to 22441CCB 22453ECB to 22476ECB 22477FCB to 22488FCB 22489GCB to 22500GCB 22511HCB to 22534HCB 22535ICB to 22558ICB 22559JCB to 22564JCB; 22570JCB to 22575JCB 22566JCB to 22569JCB; 22576JCB, 22577JCB,

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0333-2022%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.