Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Dragonfly Laryngeal Surface Electrode Recalled by Spes Medica Due to The supplier informed them of possible deviations of...
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 Spes Medica directly.
Affected Products
Dragonfly Laryngeal Surface Electrode, ET Tube Size (mm): 7.5-10.0, Channel 1, Reference Numbers LSE4246MCA075 and LSE500M. for continuous EMG monitoring of the larynx during surgical procedures.
Quantity: 20 boxes
Why Was This Recalled?
The supplier informed them of possible deviations of the parameters/processes defined for ethylene oxide sterilization.
Where Was This Sold?
This product was distributed to 3 states: CA, MA, SC
About Spes Medica
Spes Medica has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report