INTEGRATED MEDCRAFT LLC FORWARD Oral Airway Kit Recall (Unknown Date)
Announced 2026-08-12 · FDA
509 units distributed nationwide in the United States are affected. The recall covers two Guedel airway components: Size 00 (blue, product code 1100050) and Size 000 (light green, product code 1000035) with the associated lot numbers. The issue is that the devices could contain an occluded or partially occluded Guedel airway tip.
| Brand | INTEGRATED MEDCRAFT LLC |
|---|---|
| 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 | Devices could potentially contain an occluded or partially occluded Guedel Airway tip. |
| Severity | moderate |
| Units affected | 509 |
| Distribution | US Nationwide distribution. |
| Agency | FDA |
| Recall / campaign no. | FORWARD Oral Airway Kit (OPA Sizes 5, 6.5, 7, 8, 9, 10, 12). REF Number: 1011-40002. Lot Numbers: IMC-00000060, IMC-00000066, IMC-00000078, IMC-00000086, IMC-00000092, IMC-00000096, IMC-00000096, IMC-00000097, IMC-00000103, IMC-00000110, IMC-00000125, IMC-00000151, IMC-00000200, IMC-00000201, IMC-00000204, IMC-00000205. Containing the affected One-piece Guedel airway components: 1. Size 00, ISO 5.0, blue. Product Code: 1100050. Lot Numbers: 32121232, 32208193, 32400267, 32403734, 32408819, 32409672, 32416545, 32427064, 32605471, 32606405, 32606850, 32607154. 2. Size 000, ISO 3.5, light green. Product Code: 1000035. Lot Numbers: 32190425, 32213076, 32221283, 32307261, 32317627, 32321305, 32513841, 32517565 |
WHAT YOU SHOULD DO
- Do not use any Forward Oral Airway Kit units from the listed lot numbers.
- Verify whether your kit’s lot numbers match the listed ones; if yes, stop using it and contact Integrated MedCraft LLC or your supplier for return or replacement instructions.
- Retain the kit and original packaging until instructed.
- Consult a healthcare professional if the kit has been used in a procedure and follow manufacturer guidance for recall.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.