Kinetic Concepts, Inc V.A.C. X-Large Granufoam Dressing Part Numbers M6275065/5, V.A.C. ATS and V.A.C. Freedom and M6275043/5 V.A.C. Classic. Manufactured by Kinetic Concepts, Inc., San Antonio, Texas 78230 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
V.A.C. X-Large Granufoam Dressing Part Numbers M6275065/5, V.A.C. ATS and V.A.C. Freedom and M6275043/5 V.A.C. Classic. Manufactured by Kinetic Concepts, Inc., San Antonio, Texas 78230
Brand
Kinetic Concepts, Inc
Lot Codes / Batch Numbers
Part M6275043-5: 01.27.04.21v, 01.27.04.22v, 01.27.04.23v, 02.23.04.03, 05.06.04.07, 05.17.04.01, 05.20.04.08, 06.23.04.12, 07.07.04.13, and 08.11.04.04 Part M6275065-5: 11.06.03.01V, 11.06.03.02V, 11.06.03.03V, 11.21.03.15, 12.01.03.25, 12.15.03.14, 12.18.03.07, 01.16.04.09, 01.08.04.10, 01.20.04.10, 12.15.03.14, 02.04.04.23, 01.21.04.24, 02.09.04.22, 02.23.04.07, 03.30.04.13, 03.22.04.10, 05.04.04.08, 05.14.04.04, 05.26.04.09, 06.02.04.07, 06.04.04.15, 06.17.04.12, 07.07.04.11, 07.07.04.12, 07.20.04.14, 07.30.04.03, and 08.03.04.06
Products Sold
Part M6275043-5: 01.27.04.21v; 01.27.04.22v; 01.27.04.23v; 02.23.04.03; 05.06.04.07; 05.17.04.01; 05.20.04.08; 06.23.04.12; 07.07.04.13; and 08.11.04.04 Part M6275065-5: 11.06.03.01V; 11.06.03.02V; 11.06.03.03V; 11.21.03.15; 12.01.03.25; 12.15.03.14; 12.18.03.07; 01.16.04.09; 01.08.04.10; 01.20.04.10; 12.15.03.14; 02.04.04.23; 01.21.04.24; 02.09.04.22; 02.23.04.07; 03.30.04.13; 03.22.04.10; 05.04.04.08; 05.14.04.04; 05.26.04.09; 06.02.04.07; 06.04.04.15; 06.17.04.12; 07.07.04.11; 07.07.04.12; 07.20.04.14; 07.30.04.03; and 08.03.04.06
Kinetic Concepts, Inc is recalling V.A.C. X-Large Granufoam Dressing Part Numbers M6275065/5, V.A.C. ATS and V.A.C. Freedom and M627504 due to The seal on the dressing pouch may open during shipping and sterility of the dressing may be compromised.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The seal on the dressing pouch may open during shipping and sterility of the dressing may be compromised.
Recommended Action
Per FDA guidance
The firm initiated the recall by letter and phone calls on September 21, 2004.
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