Device recall
Z-0383-04: Products are various dental surgical drills packed in a sealed tray and labeled…
FDA device recall · Class II · Implant Innovations, Inc.
Key facts
| Recall number (Z-number) | Z-0383-04 |
|---|---|
| Recall event | 28092 |
| Product | Products are various dental surgical drills packed in a sealed tray and labeled as sterile. The tray is labled as follows: 3i Implant Innovations, Inc., 4555 Riverside Drive, Palm Beach 33410 USA 561-776-6700 DC500 LOT 5.0mm Implant Disposable Countersink Pilot Drill STERILE |
| Product code | DZI |
| Recalling firm | Implant Innovations, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 5, 2009 |
| FEI number | 1038806 |
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