FDA Device recall Z-2102-2025
i-view video laryngoscope
- FDA Device
- Class I
- ongoing
- Published 2025-07-23
On 2025-07-23 the FDA classified a Class I recall of i-view video laryngoscope by Intersurgical, citing potential for faulty devices as a result of depleted batteries.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2102-2025 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2025-06-17 |
| Published | 2025-07-23 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Intersurgical |
| Distribution | AZ, CA, FL, GA, IL, IN, KS, MD, MI, MO, NV, NY, OH, PA, SC, TX, VA |
Product
i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.
Reason
Potential for faulty devices as a result of depleted batteries.
Identifiers
| code_info | Model Number: 8008000. UDI-DI (Case): 05030267166497. UDI-DI (Single Unit): 5030267150649. Lot Numbers: 1240555, 1240793. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2102-2025%22
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