Device recall

Z-0045-2014: Merit Medical Performa Angiographic Catheter 5F Multipack. Part numbers 7560-43…

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

Key facts

Recall number (Z-number) Z-0045-2014
Recall event 66400
Product Merit Medical Performa Angiographic Catheter 5F Multipack. Part numbers 7560-43 and 7560-G3.
Product code DQO
Recalling firm Merit Medical Systems, Inc.
Recall class Class II
Status Terminated
Termination date Jan 3, 2014
510(k) numbers K943739
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

Browse all FDA device recalls (products)