Device recall
Z-0156-2013: Repeater Pump, Class II device used for facilitating repeatable drug dosage…
FDA device recall · Class II · Baxa Corporation
Key facts
| Recall number (Z-number) | Z-0156-2013 |
|---|---|
| Recall event | 63379 |
| Product | Repeater Pump, Class II device used for facilitating repeatable drug dosage distribution and reconstitution in hospital pharmacies. The device are Fluid Transfer Tube Sets, Sterile/EO, Std Volume Trifurcated, BAXA Corporation, Englewood, CO. The Repeater Pump is a device that provides a peristaltic… |
| Product code | NEP |
| Recalling firm | Baxa Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 15, 2013 |
| FEI number | 1419106 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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