Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LMA Esophageal Intubation Detector (EID) Recalled by LMA North America Inc Due to The recall was initiated because LMANA has received...
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 LMA North America Inc directly.
Affected Products
LMA Esophageal Intubation Detector (EID), Catalog Number EID100 The device is used to assist verification of placement of the endotracheal tube or esophageal/tracheal double lumen tube. This device is to be used as an adjunct to assess intubation. Its purpose is not to eliminate clinical judgment
Quantity: 18,799 units
Why Was This Recalled?
The recall was initiated because LMANA has received a complaint that the Esophageal Intubation Detector (EID100) has a potential to create a false positive if used on a patient during confirmation of intubation.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About LMA North America Inc
LMA North America Inc has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report