Intersurgical Recalls
11 recalls on record · December 13, 2017 to August 13, 2025 · Medical Devices
Recalls by year
17
18
20
21
22
25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
August 13, 2025Medical DevicesFDA
Intersurgical Inc recalls One-piece Guedel airway, size 3, ISO 9.0, yellow. Model Number: 1113090.
Hazard: 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.
August 13, 2025Medical DevicesFDA
Intersurgical Inc recalls One-piece Guedel airway, size 2, ISO 8.0, green. Model Number: 1112080.
Hazard: 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.
July 23, 2025Medical DevicesFDA
Intersurgical Inc recalls i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngosc
Hazard: Potential for faulty devices as a result of depleted batteries.
October 26, 2022Medical DevicesFDA
Intersurgical Inc recalls Intersurgical Solus Standard, laryngeal mask airway, size 3, small adult, 30-50kg Model Number: 8003000
Hazard: 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 the airway tube and the marking #4 on the inflation line pilot balloon) may pose health risk to the patient
January 6, 2021Medical DevicesFDA
Intersurgical Inc recalls Smoothbore breathing system with exhalation port 22 mm Device REF #: B0062001 Custom Anasthesia Breathing Systems; Multi
Hazard: The device was assembled with the incorrect exhalation port which can cause gas leakage.
January 15, 2020Medical DevicesFDA
Intersurgical Inc recalls Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3521000. Airway connector.
Hazard: The port may crack in the swivel elbow where the flip cap is inserted, and these cracks could possibly leak if they reach a significant size.
January 15, 2020Medical DevicesFDA
Intersurgical Inc recalls Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3503031. Airway connector.
Hazard: The port may crack in the swivel elbow where the flip cap is inserted, and these cracks could possibly leak if they reach a significant size.
January 15, 2020Medical DevicesFDA
Intersurgical Inc recalls Double Swivel Elbow with Bronchoscopy Port 15MM OD, 22MM OD/15MM ID, REF 1996030. Airway connector.
Hazard: The port may crack in the swivel elbow where the flip cap is inserted, and these cracks could possibly leak if they reach a significant size.
January 15, 2020Medical DevicesFDA
Intersurgical Inc recalls Double Swivel Elbow with Bronchoscopy Port 15MM OD, 22MM OD/15MM ID, REF 1898000. Airway connector.
Hazard: The port may crack in the swivel elbow where the flip cap is inserted, and these cracks could possibly leak if they reach a significant size.
July 4, 2018Medical DevicesFDA
Intersurgical Inc recalls Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm, Product No. 80062000
Hazard: When assembling an HME or Filter on this breathing circuit the tubing may be pushed up and inadvertently cover or block the exhalation port. This could potentially pose a serious health risk to the patient.
December 13, 2017Medical DevicesFDA
Intersurgical Inc recalls Solus Flexible wire-reinforced laryngeal mask airways under the following sizes: 1) small pediatric size 2 catalog #800
Hazard: A defect in the wire-reinforced tubing may result in a partial of total occlusion when the cuff is over-inflated.