Device recall
Z-1456-2013: Part510447 Disposable Infusion Pump,...Elastomeric Pump 600 mL, 2mL/hr/side…
FDA device recall · Class I · Symbios Medical Products, LLC
Key facts
| Recall number (Z-number) | Z-1456-2013 |
|---|---|
| Recall event | 65192 |
| Product | Part510447 Disposable Infusion Pump, ...Elastomeric Pump 600 mL, 2mL/hr/side,... found in the following kits GoPump Kit 510462-BP, 5 " catheter & BIOPATCH GoPump Kit 510558-BP 10 " catheter& BIOPATCH GoPump Kit 64310 Disposable Single Infusion Pump. Symbios GOPump Rapid Recovery System is 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