i-view video laryngoscope — Class I medical device recall Z-2102-2025
Ongoing recall by Intersurgical Inc, reported 2025-07-23, distributed in AZ, CA, FL, GA, IL, IN, KS, MD…. Potential for faulty devices as a result of depleted batteries.
| Recall number | Z-2102-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Intersurgical Inc, East Syracuse, NY, United States |
| Recall initiated | 2025-06-17 |
| Classified | 2025-07-11 |
| Reported by FDA | 2025-07-23 |
| Distributed | AZ, CA, FL, GA, IL, IN, KS, MD, MI, MO, NV, NY, OH, PA, SC, TX, VA |
| Quantity | 2,152 units |
| UPC / GTIN / UDI-DI | 05030267150649, 05030267166497 |
| Lot numbers | 1240555, 1240793 |
| Model numbers | 8008000 |
Product
i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.
Reason for recall
Potential for faulty devices as a result of depleted batteries.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2102-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.