Device recall

Z-0363-2019: EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A plastic container used to…

FDA device recall · Class II · Baxter Healthcare Corporation

Key facts

Recall number (Z-number) Z-0363-2019
Recall event 81240
Product EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A plastic container used to hold large-volume sterile solutions to be administered to a patient through an intravascular administration set.
Product code KPE
Recalling firm Baxter Healthcare Corporation
Recall class Class II
Status Terminated
Termination date Nov 2, 2020
510(k) numbers K900585
FEI number 1417572

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

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