Reported Jul 27, 2022 · Terminated

SX-One MicroKnife

Sonex Health LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: SONEX HEALTH LLC · 950 Blue Gentian Rd · Eagan, MN · 55121-1576

Is this the product you have?

  • SX-One MicroKnife
Lot codes and dates

3 of 3 products

Products covered by this recall
Model / numberBarcodesProduct as published
600112-001
00860002094700UDI-DI: 00860002094700
Lot Codes: 20013120, 20022821, 20022822, 20022823, 20022824, 20022825, 20070603, 20070604, 20080435, 20080436, 20083114, 20083115, 40051, 40052, 40472, 40473, 40892, 40893, 41460, 41584, 41585.
Amount recalled
3,752 devices

Where it was sold

Why it was recalled

Potential of dull blade

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 14, 2023 · Data as of Sep 19, 5:35 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.