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INTEGRATED MEDCRAFT LLC recalls FORWARD Oral Airway Kit (OPA Sizes 5, 6.5, 7, 8, 9, 10, 12). REF Number: 1011-40002. Containing the affected One-pie
Recalled August 12, 2026 · FDA recall Z-2836-2026 · INTEGRATED MEDCRAFT
Hazard
Devices could potentially contain an occluded or partially occluded Guedel Airway tip. · FDA Class II
Units
509 units
Sold at
US Nationwide distribution.
Description
Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
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.
Manufacturer(s)
INTEGRATED MEDCRAFT LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →