--- title: "Sonendo Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Sonendo 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/sonendo-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Sonendo Inc recall records **2** reported ongoing 2 records in this archive. Latest source date Oct 14, 2022. 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 Oct 14, 2022 FDA device enforcement ### [GentleWave System APM Procedure Instrument with Matrix REF GW-APM-PI02](https://isitonrecall.com/recall/fda-device-z-0233-2023-gentlewave-system-apm-procedure-instrument-with-matrix-ref-gw-apm-pi02/) Procedure Instruments with erroneous unit carton labels. Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution in the state of OH and the country of Canada. [Official source for GentleWave System APM Procedure Instrument with Matrix REF GW-APM-PI02](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0233-2023%22) Oct 14, 2022 FDA device enforcement ### [GentleWave System Posterior CleanFlow Procedure Instrument with Matrices (Single) REF GW-PST-PI01](https://isitonrecall.com/recall/fda-device-z-0234-2023-gentlewave-system-posterior-cleanflow-procedure-instrument-with-matrices-single-ref-gw-pst-pi01/) Procedure Instruments with erroneous unit carton labels. Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution in the state of OH and the country of Canada. [Official source for GentleWave System Posterior CleanFlow Procedure Instrument with Matrices (Single) REF GW-PST-PI01](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0234-2023%22) ## Reasons in these listed records - Procedure Instruments with erroneous unit carton labels. These examples come from this result page and are not a ranking of every recall reason. ## Checking Sonendo Inc ### Is there a recall on sonendo inc right now? This archive contains 2 records, including 2 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 Sonendo Inc](https://isitonrecall.com/check/?q=Sonendo%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)