Device recall
Z-2952-2026: One-Piece Guedel Airway, size 00, ISO 5.0, Blue. Oropharyngeal Airway Device.
FDA device recall · Class II · Intersurgical Inc
Key facts
| Recall number (Z-number) | Z-2952-2026 |
|---|---|
| Recall event | 99284 |
| Product | One-Piece Guedel Airway, size 00, ISO 5.0, Blue. Oropharyngeal Airway Device. |
| Product code | CAE |
| Recalling firm | Intersurgical Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 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