Drug recall
FORWARD Oral Airway Kit (OPA Sizes 5, 6.5, 7, 8, 9, 10, 12). REF Number: 1011-40002. Containing the affected…
FDA recall event 99295 · Class II · INTEGRATED MEDCRAFT LLC
Key facts
| Event ID | 99295 |
|---|---|
| Recall numbers | Z-2836-2026, Z-2837-2026 |
| Recalling firm | INTEGRATED MEDCRAFT LLC |
| Product type | Devices |
| Products | 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…, Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Containing the affected One-piece Guedel airway components: 1. Size 00, ISO 5.0, blue. Product Code: 1100050. 2. Size 000, ISO 3.5… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Devices could potentially contain an occluded or partially occluded Guedel Airway tip. |
| Initiation date | Jul 7, 2026 |
| Report date | Aug 12, 2026 |
| City | East Hampton |
| State | CT |
| Country | United States |
| FEI number | 3030078769 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: