Recall Z-2102-2025— Intersurgical Inc
Class I · Ongoing
Class I FDA medical device recall by Intersurgical Inc, initiated 2025-06-17. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Intersurgical Inc
- Classification
- Class I
- Status
- Ongoing
- Initiated
- 2025-06-17
- Firm location
- East Syracuse, NY, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.