Northgate Technologies, Inc. recalls AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe
- Recall date
- April 13, 2022
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1235-2022
- FDA classification
- Class II
- Brand / firm
- Northgate Technologies, Inc.
- Sold / distributed
- US Nationwide distribution in the state of MA.
Why it was recalled
Product labeled incorrectly.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe
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