MEDICAL DEVICE RECALLMODERATE

FORWARD Oral Airway Kit

Integrated Medcraft recalls FORWARD Oral Airway Kits due to possible occluded airway tip.

What to do

Stop using the affected FORWARD Oral Airway Kits immediately. Inspect your inventory for REF 1011-40002 and the affected Guedel components (Size 00, Product Code 1100050; Size 000, Product Code 1000035). Contact Integrated Medcraft LLC for instructions on returning the devices and obtaining replacements.

Recalled

2026-07-07

Listed

2026-07-31

Updated

2026-09-03

Recall No.

Z-2836-2026

Agency

FDA

Firm

INTEGRATED MEDCRAFT LLC

Recall ID

99295

Status

ONGOING

Recall at a glance

Quantity recalled: 509 units

Why it was recalled

Integrated Medcraft LLC is recalling FORWARD Oral Airway Kits (REF 1011-40002) containing One-piece Guedel airway components in sizes 00 and 000 because the devices could have an occluded or partially occluded airway tip, potentially impeding airflow.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

Product	Lot code	Recall #	UDI-DI
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.	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	Z-2836-2026	00000060, 00000066, 00000078, 00000086, 00000092, 00000096, 00000096, 00000097, 00000103, 00000110, 00000125, 00000151, 00000200, 00000201, 00000204, 00000205, 32121232, 32208193, 32400267, 32403734
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.	IMC-00000132, IMC-00000139, 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	Z-2837-2026	00000132, 00000139, 32121232, 32208193, 32400267, 32403734, 32408819, 32409672, 32416545, 32427064, 32605471, 32606405, 32606850, 32607154, 32190425, 32213076, 32221283, 32307261, 32317627, 32321305

Where it was sold

Distributed nationwide.

Timeline

2026-07-07Firm initiated recall
2026-07-31Publicly announced
2026-08-02Listed on Recall Canary
2026-09-03Summary updated

Official source

View on U.S. Food and Drug Administration →

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Editorial summary by Recall Canary · summary updated 2026-09-03 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification