Device recall

Z-0995-2013: KIMGUARD Container Filters, 7.5in (19cm), Round and 9in. X 9in. (23cm x 23cm)…

FDA device recall · Class II · Kimberly-Clark Corporation

Key facts

Recall number (Z-number) Z-0995-2013
Recall event 64689
Product KIMGUARD Container Filters, 7.5in (19cm), Round and 9in. X 9in. (23cm x 23cm), Square. Intended to be used to enclose another medical device that is to be sterilized by a health care provider.
Product code FRG
Recalling firm Kimberly-Clark Corporation
Recall class Class II
Status Terminated
Termination date Sep 16, 2013
510(k) numbers K881471
FEI number 1000015879

At a glance

  • 1–9 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)