Device recall

Z-3200-2017: Drill Bit Quick-Connect Calibrated 3-Fluted 2.5 mm Diameter 230 mm Length, Item…

FDA device recall · Class II · Zimmer Biomet, Inc.

Key facts

Recall number (Z-number) Z-3200-2017
Recall event 77417
Product Drill Bit Quick-Connect Calibrated 3-Fluted 2.5 mm Diameter 230 mm Length, Item Number/EDI 00480723025, Nonsterile. orthopedic surgical instrument.
Product code HWE
Recalling firm Zimmer Biomet, Inc.
Recall class Class II
Status Terminated
Termination date Mar 29, 2019
FEI number 1000220733

At a glance

  • None Linked 510(k)s
  • 10–99 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)