Device recall

Z-0070-2015: V.A.C. GranuFoam Silver Large Dressing is barrier to bacterial penetration and…

FDA device recall · Class II · KCI USA, Inc.

Key facts

Recall number (Z-number) Z-0070-2015
Recall event 69368
Product V.A.C. GranuFoam Silver Large Dressing is barrier to bacterial penetration and may help reduce infection. Featuring SensaT.R.A.C. Technology REF M8275099/10 STERILE Single Use only Latex Free Rx Only.
Product code OMP
Recalling firm KCI USA, Inc.
Recall class Class II
Status Terminated
Termination date Jul 24, 2015
FEI number 3005178245

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

Browse all FDA device recalls (products)