Device recall

Z-0508-2012: Offset Wire Fixation Bolt, catalog number 8180-50-006. The bolts are used with…

FDA device recall · Class II · DePuy Orthopaedics, Inc.

Key facts

Recall number (Z-number) Z-0508-2012
Recall event 60325
Product Offset Wire Fixation Bolt, catalog number 8180-50-006. The bolts are used with the DePuy Ace-Fischer External Fixation System and are packaged in a flexible polyethylene bag.
Product code HXK
Recalling firm DePuy Orthopaedics, Inc.
Recall class Class II
Status Terminated
Termination date Mar 7, 2013
510(k) numbers K860018
FEI number 1818910

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

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