Intersurgical Inc recalls
Every recall we track for Intersurgical Inc — 12 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Intersurgical Inc peaked in 2019 (4); 12 since 2017.
All FDA recall records for Intersurgical Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 1 | 0 | 0 | 1 |
| 2019 | 0 | 0 | 4 | 0 | 4 |
| 2020 | 0 | 0 | 1 | 0 | 1 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 1 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 1 | 2 | 0 | 3 |
| 2026 (to date) | 0 | 1 | 1 | 0 | 2 |
Most common reasons for Intersurgical Inc recalls
What to do if you have a recalled Intersurgical Inc product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Intersurgical Inc recalls
7 shown- Use cautionMedical device
Intersurgical Inc recalls One-Piece Guedel Airway, size 00, ISO 5.0, Blue. Oropharyngeal Airway Device.
Intersurgical recalls blue size 00 Guedel airway devices (ISO 5.0) due to potential occlusion. Affected units include specific lot numbers and serial codes. Consumers should contact for details.
IntersurgicalJun 15, 2026 - Lower riskMedical device
Intersurgical Inc recalls One-piece Guedel airway, size 2, ISO 8.0, green. Model Number: 1112080.
Intersurgical recalls green size 2 Guedel airways with model 1112080 due to potential small burrs that could cause airway blockage, irritation, or infection if inhaled.
IntersurgicalJun 20, 2025 - Lower riskMedical device
Intersurgical Inc recalls i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.
Intersurgical recalls i-view video laryngoscope model 8008000 due to potential battery depletion causing faulty operation. Affected units include specific lot numbers and UDI-DI codes.
IntersurgicalJun 17, 2025 - Lower riskMedical device
Intersurgical Inc recalls Intersurgical Solus Standard, laryngeal mask airway, size 3, small adult, 30-50kg Model Number: 8003000
Intersurgical recalls size 3 laryngeal mask airways with incorrect size 4 markings that may pose health risks. Affected units have model number 8003000 and lot code 32204071.
IntersurgicalAug 29, 2022 - Lower riskMedical device
Intersurgical Inc recalls Smoothbore breathing system with exhalation port 22 mm Device REF #: B0062001 Custom Anasthesia Breathing Systems;
Intersurgical recalls Smoothbore breathing systems with incorrect 22mm exhalation port (model B0062001) due to gas leakage risk during anesthesia. Affected units include lot numbers 4200283 and 4200286.
IntersurgicalNov 11, 2020 - Lower riskMedical device
Intersurgical Inc recalls Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3503031. Airway connector.
Intersurgical recalls specific Superset airway connectors due to potential port cracks that could leak. Affected units include lot numbers 2180531, 2181808, 2182241, 2182533.
IntersurgicalAug 7, 2019 - Use cautionMedical device
Intersurgical Inc recalls Flexible Smoothbore Breathing Circuit with Exhalation Port 22mm, Product No. 80062000
Intersurgical recalls flexible breathing circuits with exhalation port 22mm due to risk of blocking during assembly, potentially causing serious patient health issues. Affected units include specific product numbers listed in the recall.
IntersurgicalApr 25, 2018
Intersurgical Inc recall questions
How many recalls has Intersurgical Inc had?
12 recalls from Intersurgical Inc are on record with U.S. safety agencies, from 2018–2026.
What is the most recent Intersurgical Inc recall?
Intersurgical Inc recalls One-Piece Guedel Airway, size 00, ISO 5.0, Blue. Oropharyngeal Airway Device., dated Jun 15, 2026. Every Intersurgical Inc recall is listed on this page, newest first.
Why are Intersurgical Inc products recalled?
The most common reasons on record: Devices could potentially be occluded or partially occluded. (2).
What should I do if I have a recalled Intersurgical Inc product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Intersurgical Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.