Device recall

Z-0043-2007: Bioplate Resorbable Bone Fixation Tack, Catalog Number: 89-0120, Item Number…

FDA device recall · Class II · Bioplate Inc

Key facts

Recall number (Z-number) Z-0043-2007
Recall event 36362
Product Bioplate Resorbable Bone Fixation Tack, Catalog Number: 89-0120, Item Number: SG#-45
Product code JEY
Recalling firm Bioplate Inc
Recall class Class II
Status Terminated
Termination date Sep 14, 2011
510(k) numbers K051845
FEI number 1000518793

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 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)