--- title: "KCI USA, INC. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search KCI USA, 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/kci-usa-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # KCI USA, INC. recall records **3** reported ongoing 3 records in this archive. Latest source date Jan 17, 2025. 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 Jan 17, 2025 FDA device enforcement ### [3M Prevena Plus 125 Therapy Unit and System Kits REF: PRE3021US Prevena Plus Duo Peel and Place 20cm System Kit, US PRE3201US Prevena Plus Peel and Place 35 cm system Kit, US PR...](https://isitonrecall.com/recall/fda-device-z-1175-2025-3m-prevena-plus-125-therapy-unit-and-system-kits-ref-pre3021us-prevena-plus-duo-peel-and-place-20cm/) Due to increase in complaints related to leak alarms Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, N... [Official source for 3M Prevena Plus 125 Therapy Unit and System Kits REF: PRE3021US Prevena Plus Duo Peel and Place 2...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1175-2025%22) Jan 17, 2025 FDA device enforcement ### [3M V.A.C. VIA Negative Pressure Wound Therapy System REF: VIAKIT077D01/US - V.A.C. VIA 7 Day Kit VIAKIT07S05/AU - V.A.C. VIA Starter Kit 65-Pack VIAKIT077D01/GB - V.A.C. VIA 7 D...](https://isitonrecall.com/recall/fda-device-z-1176-2025-3m-v-a-c-via-negative-pressure-wound-therapy-system-ref-viakit077d01-us-v-a-c-via-7-day-kit-viakit07/) Due to increase in complaints related to leak alarms Class II Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, N... [Official source for 3M V.A.C. VIA Negative Pressure Wound Therapy System REF: VIAKIT077D01/US - V.A.C. VIA 7 Day Kit ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1176-2025%22) Nov 5, 2024 FDA device enforcement ### [V.A.C. Ulta Therapy Unit REF CAPULTDEV01 & ULTDEV01 The 3M" V.A.C.¿ Ulta Negative Pressure Wound Therapy System is an integrated wound management system that provides Negative P...](https://isitonrecall.com/recall/fda-device-z-0507-2025-v-a-c-ulta-therapy-unit-ref-capultdev01-ultdev01-the-3m-v-a-c-ulta-negative-pressure-wound-therapy-s/) Due to potential system error alarm and the inability to initiate therapy as a result of broken occlusion sensors. Class II Reported ongoing Distribution: Worldwide Distribution: U.S.(nationwide): AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MP, MS, MT, NC, ND, NE, NH, NJ, NM, NV,... [Official source for V.A.C. Ulta Therapy Unit REF CAPULTDEV01 & ULTDEV01 The 3M" V.A.C.¿ Ulta Negative Pressure Wound ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0507-2025%22) ## Reasons in these listed records - Due to increase in complaints related to leak alarms - Due to potential system error alarm and the inability to initiate therapy as a result of broken occlusion sensors. These examples come from this result page and are not a ranking of every recall reason. ## Checking KCI USA, INC. ### Is there a recall on kci usa, inc. right now? This archive contains 3 records, including 3 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 KCI USA, INC.](https://isitonrecall.com/check/?q=KCI%20USA%2C%20INC.) 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