Device recall

Z-1235-2025: Plato 17 Microcatheter REF PL17-160-090 To assist in delivery of therapeutic…

FDA device recall · Class II · Scientia Vascular, Inc.

Key facts

Recall number (Z-number) Z-1235-2025
Recall event 96175
Product Plato 17 Microcatheter REF PL17-160-090 To assist in delivery of therapeutic devices and embolization materials and infusion of diagnostic agents to the neuro and peripheral vasculature during interventional or diagnostic procedures.
Product code QJP
Recalling firm Scientia Vascular, Inc.
Recall class Class II
Status Open, Classified
510(k) numbers K223560
FEI number 3009546466

At a glance

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