Device recall
Z-1457-2013: Part 510449 Disposable Infusion Pump,...Elastomeric Pump 600 mL( 8mL/hr)…
FDA device recall · Class I · Symbios Medical Products, LLC
Key facts
| Recall number (Z-number) | Z-1457-2013 |
|---|---|
| Recall event | 65192 |
| Product | Part 510449 Disposable Infusion Pump, ...Elastomeric Pump 600 mL( 8mL/hr ),... found in the following kits GoBlock Kit 510472, Disposable Single Infusion Pump. Symbios GOPump Rapid Recovery System is a local pain mangagement system that consists of a small balloon that is inflated with a local… |
| Product code | MEB |
| Recalling firm | Symbios Medical Products, LLC |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 7, 2014 |
| FEI number | 3005203102 |
At a glance
- None 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