Device recall

Z-2592-2014: Split Cath III Trays, 16F x 28CM Product Usage: The Split Cath III is indicated…

FDA device recall · Class II · Medical Components, Inc dba MedComp

Key facts

Recall number (Z-number) Z-2592-2014
Recall event 68993
Product Split Cath III Trays, 16F x 28CM Product Usage: The Split Cath III is indicated for use in attaining long term vascular access for hemodialysis and apheresis in adult patients.
Product code MSD
Recalling firm Medical Components, Inc dba MedComp
Recall class Class II
Status Terminated
Termination date Dec 10, 2014
510(k) numbers K121848
FEI number 2518902

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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