Device recall

Z-0765-2023: Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF…

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

Key facts

Recall number (Z-number) Z-0765-2023
Recall event 91066
Product Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged 1/package, 20 packages/box, 12 boxes/case, sterile.
Product code KDC
Recalling firm Medical Action Industries, Inc. 306
Recall class Class II
Status Terminated
Termination date Feb 19, 2025
FEI number 1030451

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 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)