Device recall
Z-1170-2009: ReadyMed Elastomeric Ambulatory Pump, Model Numbers: R050050, R100100, R100200…
FDA device recall · Class II · Cardinal Health 303 dba Cardinal Health
Key facts
| Recall number (Z-number) | Z-1170-2009 |
|---|---|
| Recall event | 50795 |
| Product | ReadyMed Elastomeric Ambulatory Pump, Model Numbers: R050050, R100100, R100200, R250050, R250100, and R250167. Intended for self-administration of anti-microbial and antiviral agents. |
| Product code | FRN |
| Recalling firm | Cardinal Health 303 dba Cardinal Health |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 13, 2011 |
| 510(k) numbers | K895797, K913658 |
| FEI number | 2016493 |
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