Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EndoTool SubQ (Versions 1.7.1 Recalled by Monarch Medical Technologies Due to Product was distributed prior to approval or clearance...
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 Monarch Medical Technologies directly.
Affected Products
EndoTool SubQ (Versions 1.7.1, 1.7.4, 1.7.5)
Quantity: 6 units
Why Was This Recalled?
Product was distributed prior to approval or clearance from FDA.
Where Was This Sold?
This product was distributed to 4 states: CA, IL, IN, SC
About Monarch Medical Technologies
Monarch Medical Technologies has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report