Device recall
Z-1033-2009: InteliFUSE, Drill Bit, 2.00 mm, J-Latch, QTY: 1, REF: DB.200.JL, non-sterile…
FDA device recall · Class II · Intelifuse Inc
Key facts
| Recall number (Z-number) | Z-1033-2009 |
|---|---|
| Recall event | 49372 |
| Product | InteliFUSE, Drill Bit, 2.00 mm, J-Latch, QTY: 1, REF: DB.200.JL, non-sterile, 1515 Poydras st., Ste 1490, New Orleans, LA 70112, MDCI Arundel House, 1 Liverpool Gardens, Worthing, West Sussex BN11 1SL, United Kingdom Intended Use: Creating of holes for implant placement. |
| Product code | HTW |
| Recalling firm | Intelifuse Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 22, 2011 |
| FEI number | 3005509435 |
At a glance
- None 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