Device recall
Z-1366-2008: BIOMET 3i, EP Healing Abutment, REF/Item Number: THA53, 4.1mm(D) X 5mm(P) X…
FDA device recall · Class III · Biomet 3i, Inc.
Key facts
| Recall number (Z-number) | Z-1366-2008 |
|---|---|
| Recall event | 47342 |
| Product | BIOMET 3i, EP Healing Abutment, REF/Item Number: THA53, 4.1mm(D) X 5mm(P) X 3mm(H), Sterile, BIOMET 3i, Palm Beach, FL |
| Product code | NHA |
| Recalling firm | Biomet 3i, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 10, 2008 |
| 510(k) numbers | K072642 |
| 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