FORWARD Oral Airway Kit (OPA Sizes 5, 6.5, 7, 8, 9, 10, 12) recall
INTEGRATED MEDCRAFT LLC recalled FORWARD Oral Airway Kit (OPA Sizes 5, 6.5, 7, 8, 9, 10, 12) on August 12, 2026 because of devices could potentially contain an occluded or partially occluded Guedel Airway tip. It was sold nationwide.
Why it was recalled
Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
What's recalled
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.
Quantity: 509 units
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- INTEGRATED MEDCRAFT LLC, East Hampton, CT
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
US Nationwide distribution. - Status
- Ongoing
- Recall number
- Z-2836-2026
- Source
- U.S. Food and Drug Administration
More medical devices recalls
· Olympus Corporation of the AmericasMedline convenience kits containing Healthmark Instrument Channel Brushes
· Medline Industries, LPMidmark IQvitals Zone
· Midmark CorporationAchieva 3.0T; Model Numbers (REF)
· Philips North America LlcAutomated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1
· Abiomed, Inc.INCA (Infant Nasal Cannulae Assy) Neonatal Nasal CPAP, Replacement Set
· CooperSurgical, Inc.