FDA · Medical devices ·
One-Piece Guedel Airway recall
Intersurgical Inc recalled One-Piece Guedel Airway on August 26, 2026 because of devices could potentially be occluded or partially occluded. It was sold nationwide.
Why it was recalled
Devices could potentially be occluded or partially occluded.
What's recalled
One-Piece Guedel Airway, size 00, ISO 5.0, Blue. Oropharyngeal Airway Device.
Quantity: 21,269 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
- Intersurgical Inc, East Syracuse, NY
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
US Nationwide distribution in the states of CT, FL, IN, MI, OH & VA. - Status
- Ongoing
- Recall number
- Z-2952-2026
- Source
- U.S. Food and Drug Administration
More medical devices recalls
Olympus BiCOAG Hemostasis Probe 7Fr Fixed Pin Connector
· 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.
· 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.