Device recall

Z-0819-2025: AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port…

FDA device recall · Class II · Applied Medical Technology Inc

Key facts

Recall number (Z-number) Z-0819-2025
Recall event 95881
Product AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port. Model/Catalog Number: E6-1222
Product code PIF
Recalling firm Applied Medical Technology Inc
Recall class Class II
Status Completed
510(k) numbers K142989
FEI number 1526012

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)