Kinetic Concepts, Inc Sterile packaged wound dressing with white and green inner pouch and outer carton labels, labeled in part:''***V.A.C.*** ABDOMINAL DRESSING WITH NON ADHERENT LAYER***Re-Order No. M6275080/5***Manufactured for Corporate Headquarters: KCI USA, Inc., 8023 Vantage Dr., San Antonio, TX 78230 USA***''. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Sterile packaged wound dressing with white and green inner pouch and outer carton labels, labeled in part:''***V.A.C.*** ABDOMINAL DRESSING WITH NON ADHERENT LAYER***Re-Order No. M6275080/5***Manufactured for Corporate Headquarters: KCI USA, Inc., 8023 Vantage Dr., San Antonio, TX 78230 USA***''.
Brand
Kinetic Concepts, Inc
Lot Codes / Batch Numbers
Lot Codes: 05.13.05.01, 05.24.05.16, 06.09.05.24, 06.15.05.13, 07.06.05.08, 07.13.05.05.03, 07.14.05.06, 07.19.05.10, 07.28.05.15, 08.03.05.15, 08.10.05.15, 08.17.05.18, 08.17.05.30, 08.17.05.31, 09.07.05.23, 09.21.05.16, 09.28.05.16, 10.05.05.29, 10.19.05.22, 12.28.05.06, 01.11.06.16, 02.01.06.15, 02.01.06.16, 02.15.06.23, 02.15.06.24.
Products Sold
Lot Codes: 05.13.05.01; 05.24.05.16; 06.09.05.24; 06.15.05.13; 07.06.05.08; 07.13.05.05.03; 07.14.05.06; 07.19.05.10; 07.28.05.15; 08.03.05.15; 08.10.05.15; 08.17.05.18; 08.17.05.30; 08.17.05.31; 09.07.05.23; 09.21.05.16; 09.28.05.16; 10.05.05.29; 10.19.05.22; 12.28.05.06; 01.11.06.16; 02.01.06.15; 02.01.06.16; 02.15.06.23; 02.15.06.24.
Kinetic Concepts, Inc is recalling Sterile packaged wound dressing with white and green inner pouch and outer carton labels, labeled in due to Complaints received regarding difficulty opening the nonadherent layer of the device prior to application to open abdominal wounds.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Complaints received regarding difficulty opening the nonadherent layer of the device prior to application to open abdominal wounds.
Recommended Action
Per FDA guidance
Firm sent correction letters on 03/17/06 to all customers who purchased the device since May 2005.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026