Device recall
Z-1077-2009: Magic3 (Intermittent Catheter), Sterile. Hydrophilic 6 French Pediatric Length…
FDA device recall · Class II · Rochester Medical Corp
Key facts
| Recall number (Z-number) | Z-1077-2009 |
|---|---|
| Recall event | 51205 |
| Product | Magic3 (Intermittent Catheter), Sterile. Hydrophilic 6 French Pediatric Length REF 52606 Rochester Medical, Rochester Medical Corporation, Stewartville, MN 55976. Intended for use for bladder management including urine drainage, collection and measurement. |
| Product code | KOD |
| Recalling firm | Rochester Medical Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 20, 2011 |
| 510(k) numbers | K000723 |
| FEI number | 2130787 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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