Intersurgical i-view Laryngoscope Recall: Battery Depletion Risk
Intersurgical recalls i-view video laryngoscope model 8008000 due to potential battery depletion causing faulty operation. Affected units include specific lot numbers and UDI-DI codes.
Lower-risk recall
Potential for faulty devices as a result of depleted batteries.
Contact the company
What happened, in plain English
Intersurgical is recalling its i-view video laryngoscope model 8008000 because depleted batteries might cause the device to malfunction. This could lead to improper laryngoscopy during medical procedures. Read more at govinfonow.com/recall/52029-intersurgical-i-view-laryngoscope-recall-battery-depletion-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/52029-intersurgical-i-view-laryngoscope-recall-battery-depletion-risk · Updated August 17, 2026 · FDA enforcement record: FDA #Z-2102-2025
Cite this page
“Intersurgical i-view Laryngoscope Recall: Battery Depletion Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/52029-intersurgical-i-view-laryngoscope-recall-battery-depletion-risk. Based on FDA recall #Z-2102-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2102-2025%22&limit=1).
Why it’s dangerous
Depleted batteries in the i-view video laryngoscope can cause the device to malfunction during use. This might lead to improper laryngoscopy, which could affect patient safety during medical procedures.
Who’s affected
Healthcare professionals using the i-view video laryngoscope for medical procedures are most at risk. Patients undergoing laryngoscopy may be affected if the device malfunctions.
How to tell if you have this one
Check for model number 8008000 on the device. Affected units have specific lot numbers (1240555, 1240793) and UDI-DI codes (05030267166497 or 5030267150649).
- Brand
Intersurgical- Category
Medical device
What to do — step by step
Check Device Model
Look for model number 8008000 on the i-view video laryngoscope.
Verify Lot Numbers
Confirm if your device has lot numbers 1240555 or 1240793.
Where it went and when
Where it was distributed
Distributed in 17 states.
FDA distribution: “US distribution AZ, CA, FL, GA, IL, IN, KS, MD, MI, MO, NV, NY, OH, PA, SC, TX, VA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, Florida, Georgia, Illinois, Indiana, Kansas, Maryland, Michigan, Missouri, Nevada, New York, Ohio, Pennsylvania, South Carolina, Texas, Virginia.
Recall timeline
FDA published this recall 36 days after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-2102-2025 (June 17, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2102-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.