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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Device
Medical Devices/Surgical Equipment

Intersurgical i-view Video Laryngoscopes Recalled for Battery Failure Risk

Agency Publication Date: July 11, 2025
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Summary

Intersurgical Inc is recalling 2,152 i-view video laryngoscopes (Model 8008000) because the devices may have depleted batteries, which can cause the device to fail during a medical procedure. The recall affects lot numbers 1240555 and 1240793. These tools are used by healthcare professionals to see a patient's airway when inserting a breathing tube. If you possess these devices, you should stop using them and contact the manufacturer or your distributor to arrange for a return, replacement, or correction.

Risk

A depleted battery can cause the laryngoscope to fail to turn on or lose power unexpectedly during an intubation procedure. This could delay a patient's treatment, making it difficult to secure their airway and potentially leading to serious respiratory injury or death.

What You Should Do

  1. This recall affects i-view video laryngoscopes (Model 8008000) with lot numbers 1240555 and 1240793. The Unique Device Identifiers (UDI-DI) are 05030267166497 for cases and 5030267150649 for single units.
  2. Stop using the recalled laryngoscopes immediately to prevent failure during patient procedures.
  3. Contact Intersurgical Inc or your medical supply distributor to arrange for the return, replacement, or correction of the affected units.
  4. Call the FDA at 1-888-INFO-FDA (1-888-463-6332) or visit www.fda.gov/medical-devices/medical-device-recalls if you have additional questions regarding this safety alert.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: i-view video laryngoscope
Model / REF:
8008000
Lot Numbers:
1240555
1240793
UDI:
05030267166497
5030267150649

UDI-DI (Case): 05030267166497. UDI-DI (Single Unit): 5030267150649.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97121
Status: Active
Manufacturer: Intersurgical Inc
Sold By: Medical device distributors; Hospitals; Surgical centers
Manufactured In: United States
Units Affected: 2,152 pieces
Distributed To: Arizona, California, Florida, Georgia, Illinois, Indiana, Kansas, Maryland, Michigan, Missouri, Nevada, New York, Ohio, Pennsylvania, South Carolina, Texas, Virginia

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.