Device recall
Z-1452-2013: Part 510031 Disposable Single Infusion Pump, quantity Includes... TOTAL VOLUME…
FDA device recall · Class I · Symbios Medical Products, LLC
Key facts
| Recall number (Z-number) | Z-1452-2013 |
|---|---|
| Recall event | 65192 |
| Product | Part 510031 Disposable Single Infusion Pump, quantity Includes... TOTAL VOLUME: 150mL, 2 mL/hr continuous Delivery Time : App. 72 hrs when filled to capacity Sterile EO... found in the following GoPump Kits: GoPump Kit 510042, w/ Epidural Catheter GoPump Kit 510042 - BP, w/ Epidural Catheter… |
| 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