--- title: "Coapt LLC Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Coapt LLC recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/coapt-llc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Coapt LLC recall records **2** reported ongoing 2 records in this archive. Latest source date Oct 2, 2023. 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 2, 2023 FDA device enforcement ### [Coapt Dome Electrode, Gen2 system, cutaneous electrode](https://isitonrecall.com/recall/fda-device-z-0203-2024-coapt-dome-electrode-gen2-system-cutaneous-electrode/) Patient may experience minor burn or blistering if device is exposed to direct sunlight and/or warm temperatures for over 12 hours or battery is damaged. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the country of Sweden. [Official source for Coapt Dome Electrode, Gen2 system, cutaneous electrode](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0203-2024%22) Oct 2, 2023 FDA device enforcement ### [Coapt ControlSeal Electrode, cutaneous EMG Electrode](https://isitonrecall.com/recall/fda-device-z-0204-2024-coapt-controlseal-electrode-cutaneous-emg-electrode/) Patient may experience minor burn or blistering if device is exposed to direct sunlight and/or warm temperatures for over 12 hours or battery is damaged. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Canada, and Sweden. [Official source for Coapt ControlSeal Electrode, cutaneous EMG Electrode](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0204-2024%22) ## Reasons in these listed records - Patient may experience minor burn or blistering if device is exposed to direct sunlight and/or warm temperatures for over 12 hours or battery is damaged. These examples come from this result page and are not a ranking of every recall reason. ## Checking Coapt LLC ### Is there a recall on coapt llc 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 Coapt LLC](https://isitonrecall.com/check/?q=Coapt%20LLC) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)