Device recall
Z-1453-2013: Part 510076 Disposable Dual Infusion Pump,...Elastomeric Dual Pump 300 mL(150…
FDA device recall · Class I · Symbios Medical Products, LLC
Key facts
| Recall number (Z-number) | Z-1453-2013 |
|---|---|
| Recall event | 65192 |
| Product | Part 510076 Disposable Dual Infusion Pump, ...Elastomeric Dual Pump 300 mL(150 ml/side) 2mL/hr/side,... Sterile, found in the following kits: GoPump kit 510080-BP, 5 fenestrated catheter & BIOPATCH; GoPump kit 510112-BP, 2.5" fenestrated catheter & BIOPATCH Go Pump Kit 510141-BP,10" fenestrated… |
| 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