Device recall
Z-0229-04: ISPAN patient bracelet, given to patients post surgery to warn of further use of…
FDA device recall · Class II · Alcon Laboratories, Inc
Key facts
| Recall number (Z-number) | Z-0229-04 |
|---|---|
| Recall event | 27748 |
| Product | ISPAN patient bracelet, given to patients post surgery to warn of further use of dinitrogen monoxide |
| Product code | LPO |
| Recalling firm | Alcon Laboratories, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 20, 2004 |
| FEI number | 1610287 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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