medical HIGH RISK Updated 2025-07-23

Intersurgical Inc recalls i-view video laryngoscope. Model Number: 8008000. The i-

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Recalled Product

i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.

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Hazard / Issue

Potential for faulty devices as a result of depleted batteries.

Issued by

FDA

Affected States: AZ, CA, FL, GA, IL, IN, KS, MD, MI, MO, NV, NY, OH, PA, SC, TX, VA
Lot/Code Info: Model Number: 8008000. UDI-DI (Case): 05030267166497. UDI-DI (Single Unit): 5030267150649. Lot Numbers: 1240555, 1240793.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for i-view video laryngoscope. Model →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

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