KCI USA, INC.: Medical Device Recalls in 2016

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by KCI USA, INC. in 2016. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

ActiV.A.C. 300ml Canister (with Gel) for ActiV.A.C. Therapy System for the application of V.A.C. Therapy in the acute extended and home care settings. The software-controlled therapy unit applies negative pressure wound therapy. The dressing, to which the therapy unit is connected, enables distribution of the negative pressure across the surface of the wound, while the tubing transfers accumulated fluids to the canister.