Intersurgical recalls
4 official recalls and safety alerts involving Intersurgical since 2022-10, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Intersurgical or the relevant agency.
- 2026-08-26
USIntersurgical Inc recalls One-Piece Guedel Airway, size 000, ISO 3.5, Light Green. Oropharyngeal Airway Device.
Devices could potentially be occluded or partially occluded.
FDA · DeviceIntersurgical IncUS Nationwide distribution in the states of CT, FL, IN, MI, OH & VA.Official notice →- 2025-08-13
- US
Intersurgical Inc recalls One-piece Guedel airway, size 2, ISO 8.0, green. Model Number: 1112080.
Potential contamination with small burrs, which if detach could be inhaled and result in potential complications such as airway obstruction, tissue irritation, inflammation and infection.
FDA · DeviceIntersurgical IncUS distribution to AZ, CA, CT, FL, FL, HI, MA, MI, OH, UT, VA.Official notice → - 2025-07-23
- US
Intersurgical Inc recalls i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.
Potential for faulty devices as a result of depleted batteries.
FDA · DeviceIntersurgical IncUS distribution AZ, CA, FL, GA, IL, IN, KS, MD, MI, MO, NV, NY, OH, PA, SC,…Official notice → - 2022-10-26
- US
Intersurgical Inc recalls Intersurgical Solus Standard, laryngeal mask airway, size 3, small adult, 30-50kg Model Number: 8003000
Printing error on the device, size 3 Solus Standard laryngeal mask airway has been incorrectly marked with size 4 information (includes the number 4 as a size identifier, patient weight and maximum inflation volume on…