Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cobra Recalled by Neurovision Medical Products Inc Due to Mislabeling
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 Neurovision Medical Products Inc directly.
Affected Products
Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO
Quantity: 5 BOXES (25 single kits)
Why Was This Recalled?
mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Neurovision Medical Products Inc
Neurovision Medical Products Inc has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report