Device recall

Z-0811-2007: Certain MicroMiniplant Straight Healing Abutment. Dental implant. Model numbers…

FDA device recall · Class III · Biomet 3i

Key facts

Recall number (Z-number) Z-0811-2007
Recall event 37865
Product Certain MicroMiniplant Straight Healing Abutment. Dental implant. Model numbers: ISMHA32, ISMHA33, ISMHA34 and ISMHA36.
Product code DZE
Recalling firm Biomet 3i
Recall class Class III
Status Terminated
Termination date Nov 18, 2008
510(k) numbers K934126
FEI number 1038806

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)