INTEGRATED MEDCRAFT FORWARD Oral Airway Kit recall — FDA Z-2836-2026
Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
Overview of recall records associated with INTEGRATED MEDCRAFT LLC, including dates, categories and classifications where available.
Classification mix: Class II: 2.
Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
This page summarizes recall records in which the official source identifies INTEGRATED MEDCRAFT LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.