Reported Nov 20, 2019 · Terminated

EndoTool SubQ (Versions 1.7.1, 1.7.4, 1.7.5)

Monarch Medical Technologies

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: Monarch Medical Technologies · 2137 South Blvd Ste 300 · Charlotte, NC · 28203-5189

Is this the product you have?

    • EndoTool SubQ (Versions 1.7.1
    • 1.7.4
    • 1.7.5)
Lot codes and dates
  • versions
    • v 1.7.1
    • 1.7.4
    • 1.7.5
Amount recalled
6 units

Where it was sold

Why it was recalled

Product was distributed prior to approval or clearance from FDA.

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 Feb 10, 2026 · Data as of Sep 19, 5:37 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.