Device recall

Z-2605-2014: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi, LENGTH 20mm x 20mm, REF 40242020, 1 EACH…

FDA device recall · Class II · Wright Medical Technology, Inc.

Key facts

Recall number (Z-number) Z-2605-2014
Recall event 69058
Product CLAW II STRAIGHT PLATE ORTHOLOC 3DSi, LENGTH 20mm x 20mm, REF 40242020, 1 EACH, Rx ONLY, NON STERILE Orthopedic
Product code HRS
Recalling firm Wright Medical Technology, Inc.
Recall class Class II
Status Terminated
Termination date Jun 15, 2018
510(k) numbers K080295, K113014, K133715
FEI number 3010667733

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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