Device recall

Z-0564-2016: Radiographic Transparency for Certain and External Connection Tapered Implants…

FDA device recall · Class II · Biomet 3i, LLC

Key facts

Recall number (Z-number) Z-0564-2016
Recall event 72658
Product Radiographic Transparency for Certain and External Connection Tapered Implants. Images that assist with measurements for dental implants.
Product code NDP
Recalling firm Biomet 3i, LLC
Recall class Class II
Status Terminated
Termination date Dec 14, 2016
FEI number 1038806

At a glance

  • None 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

Browse all FDA device recalls (products)