Device recall
Z-3080-2026: BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris…
FDA device recall · Class I · BD SWITZERLAND SARL
Key facts
| Recall number (Z-number) | Z-3080-2026 |
|---|---|
| Recall event | 99298 |
| Product | BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter, Back Check Valve, 3 SmartSite Y-sites 10015861A 10885403232626 50885403232624 BD Alaris Pump Infusion Set, SmartSite Bag Access Non-Vented, PE Lined Tubing, Back Check Valve, 3… |
| Product code | FPA |
| Recalling firm | BD SWITZERLAND SARL |
| Recall class | Class I |
| 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