Device recall

Z-0266-2016: Biomet 3i Narrow Right Angle Large Driver Tip (Hexed). Driver tips are attached…

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

Key facts

Recall number (Z-number) Z-0266-2016
Recall event 72368
Product Biomet 3i Narrow Right Angle Large Driver Tip (Hexed). Driver tips are attached to a surgical drilling unit to carry components such as implant mounts, healing abutments and screws for placement and removal. For dental and restorative procedures.
Product code NDP
Recalling firm Biomet 3i, LLC
Recall class Class II
Status Terminated
Termination date Oct 12, 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

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