Device recall
Z-0096-2023: Intersurgical Solus Standard, laryngeal mask airway, size 3, small adult…
FDA device recall · Class II · Intersurgical Inc
Key facts
| Recall number (Z-number) | Z-0096-2023 |
|---|---|
| Recall event | 90855 |
| Product | Intersurgical Solus Standard, laryngeal mask airway, size 3, small adult, 30-50kg Model Number: 8003000 |
| Product code | CAE |
| Recalling firm | Intersurgical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 19, 2023 |
| FEI number | 1000120301 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database