Device recall
Z-1944-2024: Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2…
FDA device recall · Class II · BD SWITZERLAND SARL
Key facts
| Recall number (Z-number) | Z-1944-2024 |
|---|---|
| Recall event | 94479 |
| Product | Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite Y Sites REF 10013072 Tubing set used for delivery of fluids, medication, blood and blood products. |
| Product code | FPA |
| Recalling firm | BD SWITZERLAND SARL |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K022209 |
| FEI number | 3012798826 |
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