Intersurgical Inc issued a recall for the i-View Video Laryngoscope due to the device not turning on, battery liquid leakage, and the screen going blank, according to an FDA alert.
The i-View Video Laryngoscope is indicated for direct and indirect visualization of the larynx to facilitate oral tracheal intubation in adults.
The FDA warns that use of affected product may cause serious adverse health consequences, including trauma, desaturation, hypoxia, damage to the oropharynx, aspiration of gastric contents, and death.
As of June 20, 2025, Intersurgical has not reported any serious injuries or deaths associated with this issue, the FDA says.
Affected Product
- Product Name: i-View Video Laryngoscope
- Model Number: 8008000
- Lot/Serial Numbers: 1240555 and 1240793
FDA Recommendations
Immediately discontinue use and quarantine any affected stock. Notify customers if affected units have been further distributed.
On June 17, 2025, Intersurgical sent all affected customers an Urgent Medical Device Recall notice recommending the following actions:
- Immediately discontinue use and quarantine any affected stock.
- Immediately contact all customers, advise them of the recall situation, and have them return their outstanding recalled stock.
Customers in the US with questions about this recall should contact Intersurgical at 1-800-828-9633 or email at [email protected].
