Device recall
Z-1484-06: Alaris SE Pump (formerly Signature Edition Infusion Pump); Model Numbers: 7000…
FDA device recall · Class I · Cardinal Health 303 Inc DBA Alaris Products
Key facts
| Recall number (Z-number) | Z-1484-06 |
|---|---|
| Recall event | 36064 |
| Product | Alaris SE Pump (formerly Signature Edition Infusion Pump); Model Numbers: 7000, 7100, 7101, 7130, 7131, 7132, 7200, 7201, 7230, 7231, and 7232 |
| Product code | FRN |
| Recalling firm | Cardinal Health 303 Inc DBA Alaris Products |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jul 6, 2010 |
| 510(k) numbers | K012383, K022209, K032147 |
| FEI number | 3003879246 |
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