Total recalls 13 since 2017
Last 12 months 2 reported
Class I 1 8% of total
Ongoing 5 latest 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
Ongoing intersurgical recalls 5 active
Reported Class Recall Company Reason Where 26 Aug 2026 Device CLASS II One-Piece Guedel Airway, size 00, ISO 5.0, Blue recalled Intersurgical Other Nationwide 26 Aug 2026 Device CLASS II One-Piece Guedel Airway, size 000, ISO 3.5, Light Green recalled Intersurgical Other Nationwide 13 Aug 2025 Device CLASS II One-piece Guedel airway, size 3, ISO 9.0, yellow recalled Intersurgical Other 10 states 13 Aug 2025 Device CLASS II One-piece Guedel airway, size 2, ISO 8.0, green recalled Intersurgical Other 10 states 23 Jul 2025 Device CLASS I i-view video laryngoscope recalled by Intersurgical Intersurgical Other 17 states
All intersurgical recalls, newest first 13 total
Reported Class Recall Company Reason Where 26 Aug 2026 Device CLASS II One-Piece Guedel Airway, size 00, ISO 5.0, Blue recalled Intersurgical Other Nationwide 26 Aug 2026 Device CLASS II One-Piece Guedel Airway, size 000, ISO 3.5, Light Green recalled Intersurgical Other Nationwide 13 Aug 2025 Device CLASS II One-piece Guedel airway, size 3, ISO 9.0, yellow recalled Intersurgical Other 10 states 13 Aug 2025 Device CLASS II One-piece Guedel airway, size 2, ISO 8.0, green recalled Intersurgical Other 10 states 23 Jul 2025 Device CLASS I i-view video laryngoscope recalled by Intersurgical Intersurgical Other 17 states 26 Oct 2022 Device CLASS II Solus Standard, laryngeal mask airway, size 3, small adult recalled Intersurgical Other OH, TN, TX 6 Jan 2021 Device CLASS II Smoothbore breathing system with exhalation port Device recalled Intersurgical Packaging Defects NY 15 Jan 2020 Device CLASS II Superset with ID, Double Swivel Elbow OD/ ID and Bronchoscopy Port recalled Intersurgical Packaging Defects Nationwide 15 Jan 2020 Device CLASS II Double Swivel Elbow with Bronchoscopy Port OD/ ID recalled Intersurgical Packaging Defects Nationwide 15 Jan 2020 Device CLASS II Double Swivel Elbow with Bronchoscopy Port OD/ ID recalled Intersurgical Packaging Defects Nationwide 15 Jan 2020 Device CLASS II Superset with ID, Double Swivel Elbow OD/ ID and Bronchoscopy Port recalled Intersurgical Packaging Defects Nationwide 4 Jul 2018 Device CLASS II Flexible Smoothbore Breathing Circuit with Exhalation Port recalled Intersurgical Other 5 states 13 Dec 2017 Device CLASS II Solus Flexible wire-reinforced laryngeal mask airways under recalled Intersurgical Device Malfunction 5 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.