Device recall
Z-2836-2026: FORWARD Oral Airway Kit (OPA Sizes 5, 6.5, 7, 8, 9, 10, 12). REF Number…
FDA device recall · Class II · INTEGRATED MEDCRAFT LLC
Key facts
| Recall number (Z-number) | Z-2836-2026 |
|---|---|
| Recall event | 99295 |
| Product | FORWARD Oral Airway Kit (OPA Sizes 5, 6.5, 7, 8, 9, 10, 12). REF Number: 1011-40002. Containing the affected One-piece Guedel airway components: 1. Size 00, ISO 5.0, blue. Product Code: 1100050. 2. Size 000, ISO 3.5, light green. Product Code: 1000035. |
| Product code | CAE |
| Recalling firm | INTEGRATED MEDCRAFT LLC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3030078769 |
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