Device recall

Z-0523-2010: Merit Medical Sysems, Inc. Pressure Infusor Bag MERITMEDICAL 500 ml Pressure…

FDA device recall · Class II · Merit Medical Systems, Inc.

Key facts

Recall number (Z-number) Z-0523-2010
Recall event 53557
Product Merit Medical Sysems, Inc. Pressure Infusor Bag MERITMEDICAL 500 ml Pressure Infusor Bag CATALOG NUMBER PIB500 Used to apply pressure to a sealed bag of sterile fluid.
Product code KZD
Recalling firm Merit Medical Systems, Inc.
Recall class Class II
Status Terminated
Termination date Dec 15, 2009
FEI number 1721504

At a glance

  • None Linked 510(k)s
  • 10–99 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)