Intersurgical recalls

Intersurgical has 13 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 26 Aug 2026. 5 are still ongoing. 2 were reported in the last 12 months.

Total recalls13since 2017
Last 12 months2reported
Class I18% of total
Ongoing5latest 26 Aug 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 1 8%Class II 12 92%Class III 0 0%

Why intersurgical is recalled

By year

Ongoing intersurgical recalls

5 active
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIOne-Piece Guedel Airway, size 00, ISO 5.0, Blue recalledIntersurgicalOtherNationwide
DeviceCLASS IIOne-Piece Guedel Airway, size 000, ISO 3.5, Light Green recalledIntersurgicalOtherNationwide
DeviceCLASS IIOne-piece Guedel airway, size 3, ISO 9.0, yellow recalledIntersurgicalOther10 states
DeviceCLASS IIOne-piece Guedel airway, size 2, ISO 8.0, green recalledIntersurgicalOther10 states
DeviceCLASS Ii-view video laryngoscope recalled by IntersurgicalIntersurgicalOther17 states

All intersurgical recalls, newest first

13 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIOne-Piece Guedel Airway, size 00, ISO 5.0, Blue recalledIntersurgicalOtherNationwide
DeviceCLASS IIOne-Piece Guedel Airway, size 000, ISO 3.5, Light Green recalledIntersurgicalOtherNationwide
DeviceCLASS IIOne-piece Guedel airway, size 3, ISO 9.0, yellow recalledIntersurgicalOther10 states
DeviceCLASS IIOne-piece Guedel airway, size 2, ISO 8.0, green recalledIntersurgicalOther10 states
DeviceCLASS Ii-view video laryngoscope recalled by IntersurgicalIntersurgicalOther17 states
DeviceCLASS IISolus Standard, laryngeal mask airway, size 3, small adult recalledIntersurgicalOtherOH, TN, TX
DeviceCLASS IISmoothbore breathing system with exhalation port Device recalledIntersurgicalPackaging DefectsNY
DeviceCLASS IISuperset with ID, Double Swivel Elbow OD/ ID and Bronchoscopy Port recalledIntersurgicalPackaging DefectsNationwide
DeviceCLASS IIDouble Swivel Elbow with Bronchoscopy Port OD/ ID recalledIntersurgicalPackaging DefectsNationwide
DeviceCLASS IIDouble Swivel Elbow with Bronchoscopy Port OD/ ID recalledIntersurgicalPackaging DefectsNationwide
DeviceCLASS IISuperset with ID, Double Swivel Elbow OD/ ID and Bronchoscopy Port recalledIntersurgicalPackaging DefectsNationwide
DeviceCLASS IIFlexible Smoothbore Breathing Circuit with Exhalation Port recalledIntersurgicalOther5 states
DeviceCLASS IISolus Flexible wire-reinforced laryngeal mask airways under recalledIntersurgicalDevice Malfunction5 states

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.