Device recall
Z-0940-2013: GOPump Elastometric infusion PumpKit with/ and without accesssories all…
FDA device recall · Class I · Symbios Medical Products, LLC
Key facts
| Recall number (Z-number) | Z-0940-2013 |
|---|---|
| Recall event | 64423 |
| Product | GOPump Elastometric infusion PumpKit with/ and without accesssories all containing Dual GOPump, part number 510076: One infusion pump comprising two, 150 mL elastomeric reservoirs, each of which connects to its own catheter. Liquid flow rate is labeled at 2 mL/hr per elastomer. The Symbios… |
| Product code | MEB |
| Recalling firm | Symbios Medical Products, LLC |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Feb 13, 2014 |
| 510(k) numbers | K072921 |
| FEI number | 3005203102 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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