Northgate Technologies, Inc. AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe
Brand
Northgate Technologies, Inc.
Lot Codes / Batch Numbers
NTI Catalog Number 72-00322-0 / BSC Catalog No. M00546620, Lot code: BSC15876, GTIN: 00817183020448.
Products Sold
NTI Catalog Number 72-00322-0 / BSC Catalog No. M00546620; Lot code: BSC15876; GTIN: 00817183020448.
Northgate Technologies, Inc. is recalling AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe due to Product labeled incorrectly.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Product labeled incorrectly.
Recommended Action
Per FDA guidance
The firm sent out the recall notification to their consignee on 04/13/2022 via email. The firm sent out a letter as well on 04/27/2022 which instructs the consignee to cease distribution, quarantine affected units and return affected product. If the distributor further distributed the product, they are asked to notify their customers.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026