--- title: "Intersurgical Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Intersurgical Inc recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/intersurgical-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Intersurgical Inc recall records **5** reported ongoing 6 records in this archive. Latest source date Jun 15, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Jun 15, 2026 FDA device enforcement ### [One-Piece Guedel Airway, size 00, ISO 5.0, Blue. Oropharyngeal Airway Device.](https://isitonrecall.com/recall/fda-device-z-2952-2026-one-piece-guedel-airway-size-00-iso-5-0-blue-oropharyngeal-airway-device/) Devices could potentially be occluded or partially occluded. Class II Reported ongoing Distribution: US Nationwide distribution in the states of CT, FL, IN, MI, OH & VA. [Official source for One-Piece Guedel Airway, size 00, ISO 5.0, Blue. Oropharyngeal Airway Device.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2952-2026%22) Jun 15, 2026 FDA device enforcement ### [One-Piece Guedel Airway, size 000, ISO 3.5, Light Green. Oropharyngeal Airway Device.](https://isitonrecall.com/recall/fda-device-z-2953-2026-one-piece-guedel-airway-size-000-iso-3-5-light-green-oropharyngeal-airway-device/) Devices could potentially be occluded or partially occluded. Class II Reported ongoing Distribution: US Nationwide distribution in the states of CT, FL, IN, MI, OH & VA. [Official source for One-Piece Guedel Airway, size 000, ISO 3.5, Light Green. Oropharyngeal Airway Device.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2953-2026%22) Jun 20, 2025 FDA device enforcement ### [One-piece Guedel airway, size 2, ISO 8.0, green. Model Number: 1112080.](https://isitonrecall.com/recall/fda-device-z-2275-2025-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. Class II Reported ongoing Distribution: US distribution to AZ, CA, CT, FL, FL, HI, MA, MI, OH, UT, VA. [Official source for One-piece Guedel airway, size 2, ISO 8.0, green. Model Number: 1112080.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2275-2025%22) Jun 20, 2025 FDA device enforcement ### [One-piece Guedel airway, size 3, ISO 9.0, yellow. Model Number: 1113090.](https://isitonrecall.com/recall/fda-device-z-2276-2025-one-piece-guedel-airway-size-3-iso-9-0-yellow-model-number-1113090/) 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. Class II Reported ongoing Distribution: US distribution to AZ, CA, CT, FL, FL, HI, MA, MI, OH, UT, VA. [Official source for One-piece Guedel airway, size 3, ISO 9.0, yellow. Model Number: 1113090.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2276-2025%22) Jun 17, 2025 FDA device enforcement ### [i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.](https://isitonrecall.com/recall/fda-device-z-2102-2025-i-view-video-laryngoscope-model-number-8008000-the-i-view-video-laryngoscope-is-indicated-to-facilit/) Potential for faulty devices as a result of depleted batteries. Class I Reported ongoing Distribution: US distribution AZ, CA, FL, GA, IL, IN, KS, MD, MI, MO, NV, NY, OH, PA, SC, TX, VA. [Official source for i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to f...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2102-2025%22) Aug 29, 2022 FDA device enforcement ### [Intersurgical Solus Standard, laryngeal mask airway, size 3, small adult, 30-50kg Model Number: 8003000](https://isitonrecall.com/recall/fda-device-z-0096-2023-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 the airway tube and the marking #4 on t... Class II Reported terminated Distribution: OH, TN, TX [Official source for Intersurgical Solus Standard, laryngeal mask airway, size 3, small adult, 30-50kg Model Number: 8...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0096-2023%22) ## Reasons in these listed records - Devices could potentially be occluded or partially occluded. - 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. - Potential for faulty devices as a result of depleted batteries. - 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 pi... These examples come from this result page and are not a ranking of every recall reason. ## Checking Intersurgical Inc ### Is there a recall on intersurgical inc right now? This archive contains 6 records, including 5 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Intersurgical Inc](https://isitonrecall.com/check/?q=Intersurgical%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)