Device recall
Z-1215-2012: Integra CUSA EXcel Sterile Tips Rx Only Single Use Only Product Usage: For usage…
FDA device recall · Class II · Integra LifeSciences Corp
Key facts
| Recall number (Z-number) | Z-1215-2012 |
|---|---|
| Recall event | 61093 |
| Product | Integra CUSA EXcel Sterile Tips Rx Only Single Use Only Product Usage: For usage in surgical procedures where fragmentation, emulsification and aspiration of soft and hard (e.g. bone) tissue is desirable. |
| Product code | LFL |
| Recalling firm | Integra LifeSciences Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 19, 2012 |
| 510(k) numbers | K981262 |
| FEI number | 1121308 |
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