KCI USA, INC. 2025-02-26 Health serious FDA
Health · FDA · Recall #FDA-Z-1176-2025
3M V.A.C. VIA Negative Pressure Wound Therapy System REF: VIAKIT077D01/US - V.A.C. VIA… Recall
Issued February 26, 2025 · KCI USA, INC.
In February 2025, KCI USA, INC. recalled the 3M V.A.C. VIA Negative Pressure Wound Therapy System REF: VIAKIT077D01/US - V.A.C. VIA…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Due to increase in complaints related to leak alarms
What you should do
- 1 Stop using 3M V.A.C. VIA Negative Pressure Wound Therapy System REF: VIAKIT077D01/US - V.A.C. VIA… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact KCI USA, INC. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- KCI USA, INC.
- Category
- Health
- Recall date
- February 26, 2025
- Units affected
- Not reported
- Sold at
- 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,
- Recall number
- FDA-Z-1176-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- KCI USA, INC. has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.