Device recall

Z-1476-2018: ZMS Intramedullary Fixation Smooth Guide Wire Bullet Tip 3.0 mm Diameter, 100 cm…

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

Key facts

Recall number (Z-number) Z-1476-2018
Recall event 79681
Product ZMS Intramedullary Fixation Smooth Guide Wire Bullet Tip 3.0 mm Diameter, 100 cm Length; Item Number: 47-2237-038-00
Product code LXH
Recalling firm Zimmer Biomet, Inc.
Recall class Class II
Status Terminated
Termination date Nov 18, 2020
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)