FDA recall, , Moderate risk
FORWARD Oral Airway Kit and Kingfisher Compact Individual First Aid Kit
The FORWARD Oral Airway Kit may have an occluded or partially occluded Guedel Airway tip.
Summary by Recall Canary from the FDA notice
What happened
INTEGRATED MEDCRAFT LLC of East Hampton, Connecticut, recalled the FORWARD Oral Airway Kit and the Kingfisher Compact Individual First Aid Kit because the devices could potentially contain an occluded or partially occluded Guedel Airway tip. The kits include affected One-piece Guedel airway components in sizes 00 (ISO 5.0, blue) and 000 (ISO 3.5, light green).
The recall began July 7, 2026, and was added to the FDA's Enforcement Report on July 31, 2026. The products were distributed nationwide in the US.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your kit affected?
Compare the details below with your product and check the FDA notice to confirm whether it is affected.
A UDI-DI is the device identifier printed with the barcode on the device label.
Product details
Kingfisher Compact Individual First Aid Kit. REF Number: 76656. 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.
- UDI-DI
- 00000132
- 00000139
- 32121232
- 32208193
- 32400267
- 32403734
- 32408819
- 32409672
- 32416545
- 32427064
- 32605471
- 32606405
- 32606850
- 32607154
- 32190425
- 32213076
- 32221283
- 32307261
- 32317627
- 32321305
- 32513841
- 32517565
- Lot code
- IMC-00000132
- IMC-00000139
- 5.0
- 1100050
- 000
- 3.5
- 1000035
Product details
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.
- UDI-DI
- 00000060
- 00000066
- 00000078
- 00000086
- 00000092
- 00000096
- 00000097
- 00000103
- 00000110
- 00000125
- 00000151
- 00000200
- 00000201
- 00000204
- 00000205
- 32121232
- 32208193
- 32400267
- 32403734
- 32408819
- 32409672
- 32416545
- 32427064
- 32605471
- 32606405
- 32606850
- 32607154
- 32190425
- 32213076
- 32221283
- 32307261
- 32317627
- 32321305
- 32513841
- 32517565
- Affected units
- 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, 5.0, 1100050, 32121232, 32208193, 32400267, 32403734, 32408819, 32409672, 32416545, 32427064, 32605471, 32606405, 32606850, 32607154, 000, 3.5, 1000035, 32190425, 32213076, 32221283, 32307261, 32317627, 32321305, 32513841, 32517565
Recall details
- Company began the recall
- Sold in
US Nationwide distribution.
- Company
- INTEGRATED MEDCRAFT LLCEast Hampton, Connecticut
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99295
- Recall numbers
- Z-2836-2026 to Z-2837-2026
All recalls from INTEGRATED MEDCRAFT LLC
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
