Device recall

Z-1811-2014: Biomet Spine, Cypher MIS Screw Inserter, Catalog number 14-501669, instrument…

FDA device recall · Class II · Ebi, Llc

Key facts

Recall number (Z-number) Z-1811-2014
Recall event 68526
Product Biomet Spine, Cypher MIS Screw Inserter, Catalog number 14-501669, instrument for Spinal Screw Fixation System.
Product code HXX
Recalling firm Ebi, Llc
Recall class Class II
Status Terminated
Termination date Apr 21, 2017
FEI number 2242816

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)