Device recall

Z-0551-05: Arrow PICC Kit with Blue Flex Tip Catheter and Placement Wire. Catalog number…

FDA device recall · Class II · Arrow International Inc

Key facts

Recall number (Z-number) Z-0551-05
Recall event 30089
Product Arrow PICC Kit with Blue Flex Tip Catheter and Placement Wire. Catalog number PK-01552-WSSP
Product code LJS
Recalling firm Arrow International Inc
Recall class Class II
Status Terminated
Termination date May 4, 2005
510(k) numbers K930129
FEI number 3015859709

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)