Device recall

Z-1394-2024: IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case…

FDA device recall · Class II · Medical Action Industries, Inc. 306

Key facts

Recall number (Z-number) Z-1394-2024
Recall event 94181
Product IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.
Product code LRS
Recalling firm Medical Action Industries, Inc. 306
Recall class Class II
Status Open, Classified
FEI number 1030451

At a glance

  • None 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)