FDA Device recall Z-1235-2022
AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe
- FDA Device
- Class II
- terminated
- Published 2022-06-15
On 2022-06-15 the FDA classified a Class II recall of AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe by Northgate Technologies, citing product labeled incorrectly.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1235-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-04-13 |
| Published | 2022-06-15 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Northgate Technologies |
| Distribution | US |
Product
AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe
Reason
Product labeled incorrectly.
Identifiers
| code_info | NTI Catalog Number 72-00322-0 / BSC Catalog No. M00546620; Lot code: BSC15876; GTIN: 00817183020448. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1235-2022%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.