3M V — Class II medical device recall Z-1176-2025

Ongoing recall by KCI USA, INC., reported 2025-02-26, distributed nationwide. Due to increase in complaints related to leak alarms

Recall number	`Z-1176-2025`
Product type	Medical device
Classification	Class II
Status	Ongoing
Voluntary or mandated	Voluntary
Recalling firm	KCI USA, INC., San Antonio, TX, United States
Recall initiated	2025-01-17
Classified	2025-02-14
Reported by FDA	2025-02-26
Distributed	Nationwide (US)
Countries outside the US	AE, AT, AU, BE, BH, BR, CA, CH, CL, CN, CO, CY, DE, DK, ES, FI, FR, GB, GR, IE, IT, JO, JP, KW, MX, NL, NO, NZ, OM, QA, SA, SE, SG, TR, ZA
Quantity	2,169
Reason classes	packaging
UPC / GTIN / UDI-DI	`00849554002364`, `00849554002388`, `00849554002401`
Lot numbers	`C16936V003`, `C16937V003`, `C17027V003`, `C17525V003`, `C17557V003`, `VIAKIT077D01/GB`, `VIAKIT07S05/AU`
Model numbers	`VIAKIT077D01/GBV003`, `VIAKIT077D01/US`, `VIAKIT077D01/USV003`, `VIAKIT07S05/AU`, `VIAKIT07S05/AUV003`

Product

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 Day Kit, Single Shipper

Reason for recall

Due to increase in complaints related to leak alarms

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1176-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.