Recall Z-2953-2026— Intersurgical Inc
Class II · Ongoing
Class II FDA medical device recall by Intersurgical Inc, initiated 2026-06-15. FDA's recall record names no specific 510(k) clearance for this event. Product: One-Piece Guedel Airway, size 000, ISO 3.5, Light Green. Oropharyngeal Airway Device.. Reason: Devices could potentially be occluded or partially occluded..
- Recalling firm
- Intersurgical Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-06-15
- Firm location
- East Syracuse, NY, United States
Product description
One-Piece Guedel Airway, size 000, ISO 3.5, Light Green. Oropharyngeal Airway Device.
Reason for recall
Devices could potentially be occluded or partially occluded.
Data sourced from openFDA. This site is unofficial and independent of the FDA.