Recall Z-2102-2025
Intersurgical Inc · initiated June 17, 2025
Class I – dangerous or defective products that could cause serious health problems or death
Product
i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.
Codes / lots: Model Number: 8008000. UDI-DI (Case): 05030267166497. UDI-DI (Single Unit): 5030267150649. Lot Numbers: 1240555, 1240793.
Reason for recall
Potential for faulty devices as a result of depleted batteries.
FDA-determined cause: Component design/selection
Action taken
Intersurgical notified consignees and account executives via email on 06/17/2025. The notification instructed consignees and account executives to immediately discontinue use and quarantine any affected stock on hand, notify customers if affected units have been further distributed, and contact Intersurgical Customer Support at 800-828-9633 for a Return Goods Authorization (RGA) Number and return label to return all affected units. Also, they were instructed to complete and return the Customer Product Recall Acknowledgement Form.
Details
- Recall number
- Z-2102-2025
- Initiated
- June 17, 2025
- Posted by FDA
- July 11, 2025
- Product code
- CCW – Laryngoscope, Rigid
- Quantity
- 2,152 pieces
- Distribution
- US distribution AZ, CA, FL, GA, IL, IN, KS, MD, MI, MO, NV, NY, OH, PA, SC, TX, VA.
- Recalling firm
- Intersurgical Inc, East Syracuse, NY