FDA Medical devices recall ·
i-view video laryngoscope recall
This is an FDA Class I recall — the most serious type.
- Recall number
- Z-2102-2025
- Date
- (initiated June 17, 2025)
- Company / brand
- Intersurgical Inc
5010 Campuswood Dr Ste 102, East Syracuse, NY, United States - Category
- Medical devices › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 2,152 pieces
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.
Why was it recalled?
Potential for faulty devices as a result of depleted batteries.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Model Number: 8008000. UDI-DI (Case): 05030267166497. UDI-DI (Single Unit): 5030267150649. Lot Numbers: 1240555, 1240793.
Distribution
US distribution AZ, CA, FL, GA, IL, IN, KS, MD, MI, MO, NV, NY, OH, PA, SC, TX, VA.
States: Arizona California Florida Georgia Illinois Indiana Kansas Maryland Michigan Missouri Nevada New York Ohio Pennsylvania South Carolina Texas Virginia
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (medical devices), recall Z-2102-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.