Device recall

Z-0094-2015: Continuum Acetabular System Trabecular Metal Shell with Multi Holes, Porous…

FDA device recall · Class II · Zimmer, Inc.

Key facts

Recall number (Z-number) Z-0094-2015
Recall event 69301
Product Continuum Acetabular System Trabecular Metal Shell with Multi Holes, Porous 68mm, Prosthesis, Hip, Semi-Constrained, Metal/Polymer
Product code JDI
Recalling firm Zimmer, Inc.
Recall class Class II
Status Terminated
Termination date Mar 2, 2015
510(k) numbers K091508
FEI number 1000220733

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

Browse all FDA device recalls (products)