Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope Recalled by Intersurgical Inc Due to Potential for faulty devices as a result 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 Intersurgical Inc directly.
Affected Products
i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.
Quantity: 2,152 pieces
Why Was This Recalled?
Potential for faulty devices as a result of depleted batteries.
Where Was This Sold?
This product was distributed to 17 states: AZ, CA, FL, GA, IL, IN, KS, MD, MI, MO, NV, NY, OH, PA, SC, TX, VA
About Intersurgical Inc
Intersurgical 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