Device recall

Z-0162-2015: Merit Maestro Microcatheter, 2.4F 130cm Straight, REF28MC24130ST, Rx Only…

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

Key facts

Recall number (Z-number) Z-0162-2015
Recall event 69452
Product Merit Maestro Microcatheter, 2.4F 130cm Straight, REF28MC24130ST, Rx Only, Non-pyrogenic Sterile if package is unopened or undamaged.
Product code KRA
Recalling firm Merit Medical Systems, Inc.
Recall class Class II
Status Terminated
Termination date Nov 19, 2014
510(k) numbers K082613
FEI number 1721504

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 100–999 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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