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Monarch Medical Technologies recalls EndoTool SubQ (Versions 1.7.1, 1.7.4, 1.7.5)
Recalled November 20, 2019 · FDA recall Z-0354-2020 · Monarch Medical Technologies
Hazard
Product was distributed prior to approval or clearance from FDA. · FDA Class II
Units
6 units
Sold at
SC, IL IN, CA
Description
Product was distributed prior to approval or clearance from FDA.
Product
EndoTool SubQ (Versions 1.7.1, 1.7.4, 1.7.5)
Manufacturer(s)
Monarch Medical Technologies
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →