Device recall

Z-0475-2014: Zimmer Trabecular Metal Total Ankle Talar Component Left Sizes 1-6 Total ankle…

FDA device recall · Class II · Zimmer, Inc.

Key facts

Recall number (Z-number) Z-0475-2014
Recall event 66717
Product Zimmer Trabecular Metal Total Ankle Talar Component Left Sizes 1-6 Total ankle arthroplasty is intended to provide a patient with limited mobility by restoring alignment, reducing pain and preserving the flexion/extension movement within the ankle joint.The Zimmer Trabecular Metal Total Ankle is…
Product code HSN
Recalling firm Zimmer, Inc.
Recall class Class II
Status Terminated
Termination date Oct 15, 2014
510(k) numbers K120906
FEI number 1000220733

At a glance

  • 1–9 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

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