# FDA device recall: FORWARD Oral Airway Kit (OPA Sizes 5, 6.5, 7, 8, 9, 10, 12). REF Number: 1011-40002.     Containing the affected One-pie

> recall · VERIFIED · 2026-07-07

Firm: INTEGRATED MEDCRAFT LLC · Class II · Devices could potentially contain an occluded or partially occluded Guedel Airway tip.

- Company: INTEGRATED MEDCRAFT LLC
- Sector: medical devices
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.