Every recall we track for KCI USA, INC. — 4 in all — plus the complaints and injury reports the public filed about them.
3M recalls Prevena Plus therapy units and system kits due to potential leak alarms not functioning properly. Affected units include specific model numbers and lot numbers listed in the recall notice.
3M recalls specific V.A.C. VIA Negative Pressure Wound Therapy kits due to leak alarms. Affected kits include VIAKIT077D01/US and VIAKIT07S05/AU models with certain lot numbers. Consumers should check their kit's UDI-DI code and lot numbers for recall.
KCI recalls V.A.C. Ulta Therapy Units with model CAPULTDEV01 and serial numbers GAAC06245-GAAC20993 due to potential system error alarms and inability to initiate therapy from broken occlusion sensors.
KCI recalls ACTIV.A.C Therapy System models from 2007-2020 with software up to 3.11 due to risk of stopping negative pressure wound therapy without user notification.
