Device recall
Z-0933-03: Gravity and Infusion Pump Intravenous (IV) Sets using the Y-site Ultrasite Valve…
FDA device recall · Class II · Braun,B Medical Inc
Key facts
| Recall number (Z-number) | Z-0933-03 |
|---|---|
| Recall event | 26226 |
| Product | Gravity and Infusion Pump Intravenous (IV) Sets using the Y-site Ultrasite Valve including: Horizon Pump IV Sets; Vista Pump IV Sets; Primary IV Sets; Blood Sets; Burette Sets; Filtered Administration Sets; Extension Sets; Anesthesia Sets; Rate Flow Extension Sets; and Rate Flow IV Administration… |
| Product code | FPA |
| Recalling firm | Braun,B Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 29, 2004 |
| 510(k) numbers | K760383 |
| FEI number | 2523676 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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