Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe Recalled by Northgate Technologies, Inc. Due to Product labeled incorrectly.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Northgate Technologies, Inc. directly.
Affected Products
AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe
Quantity: 55 probes
Why Was This Recalled?
Product labeled incorrectly.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Northgate Technologies, Inc.
Northgate Technologies, Inc. has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report