AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic recall
AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe
Why was AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic recalled?
Product labeled incorrectly.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
NTI Catalog Number 72-00322-0 / BSC Catalog No. M00546620; Lot code: BSC15876; GTIN: 00817183020448.
- Product
- AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe
- Recalling firm
- Northgate Technologies, Inc.
- Quantity
- 55 probes
- Distribution
- US Nationwide distribution in the state of MA.
- Recall date
- June 15, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)