# FDA recall Z-1176-2025

> **KCI USA, INC.** · Class II · device recall initiated 2025-01-17.

## 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

## 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, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV and WY.  The countries of Australia, Austria, Bahrain, Belgium, Brazil, Canada, Chile, China, Colombia, Cyprus, Denmark, Finland, France, Germany, Greece, Ireland, Italy, Japan, Jordan, Kuwait, Mexico, Netherlands, New Zealand, Norway, Oman, Qatar, Saudi Arabia, Singapore, South Africa, Spain, Sweden, Switzerland, Turkey, UAE and UK.

## Key facts

- **Recall number:** Z-1176-2025
- **Recalling firm:** KCI USA, INC.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-01-17
- **Report date:** 2025-02-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Antonio, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1176-2025

## Citation

> AI Analytics. FDA recall Z-1176-2025. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1176-2025. Source: US FDA. Licensed CC0.

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