Device recall
Z-0659-03: TPS-TL Straight Drill Guide Applicator, Catalog Number 1300-9016.
FDA device recall · Class II · Interpore Cross International Inc
Key facts
| Recall number (Z-number) | Z-0659-03 |
|---|---|
| Recall event | 25628 |
| Product | TPS-TL Straight Drill Guide Applicator, Catalog Number 1300-9016. |
| Product code | LXH |
| Recalling firm | Interpore Cross International Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 28, 2003 |
| FEI number | 1000160576 |
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