Device recall

Z-2059-2015: Altiva / Exactech Spine, Large Set Screw, Catalog Number 28202, Lot Number…

FDA device recall · Class II · Exactech, Inc.

Key facts

Recall number (Z-number) Z-2059-2015
Recall event 71528
Product Altiva / Exactech Spine, Large Set Screw, Catalog Number 28202, Lot Number AS05107. Intended to provide immobilization and stabilization of spinal segments.
Product code MNH
Recalling firm Exactech, Inc.
Recall class Class II
Status Terminated
Termination date Jul 14, 2015
510(k) numbers K051216
FEI number 1038671

At a glance

  • 1–9 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)