Device recall

Z-0559-04: 4mm Hex Driver

FDA device recall · Class II · U&I America

Key facts

Recall number (Z-number) Z-0559-04
Recall event 28163
Product 4mm Hex Driver
Product code MNI
Recalling firm U&I America
Recall class Class II
Status Terminated
Termination date Mar 24, 2004
510(k) numbers K020279, K024096, K031585, K031595
FEI number 3003200830

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

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