FORWARD Oral Airway Kit — Class II medical device recall Z-2836-2026
Ongoing recall by INTEGRATED MEDCRAFT LLC, reported 2026-08-12, distributed nationwide. Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
| Recall number | Z-2836-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | INTEGRATED MEDCRAFT LLC, East Hampton, CT, United States |
| Recall initiated | 2026-07-07 |
| Classified | 2026-07-31 |
| Reported by FDA | 2026-08-12 |
| Distributed | Nationwide (US) |
| Quantity | 509 units |
| Lot numbers | 32121232, 32190425, 32208193, 32213076, 32221283, 32307261, 32317627, 32321305, 32400267, 32403734, 32408819, 32409672, 32416545, 32427064, 32513841, 32517565, 32605471, 32606405, 32606850, 32607154, IMC-00000060, IMC-00000066, IMC-00000078, IMC-00000086, IMC-00000092, IMC-00000096, IMC-00000097, IMC-00000103, IMC-00000110, IMC-00000125, IMC-00000151, IMC-00000200, IMC-00000201, IMC-00000204, IMC-00000205 |
| Model numbers | 1011-40002 |
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.
Reason for recall
Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2836-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.