Device recall
Z-1770-2019: Alaris Pump Infusion Set, Model Codes 10010453, 10010454, 10012144, 10015294…
FDA device recall · Class I · Becton Dickinson & Company
Key facts
| Recall number (Z-number) | Z-1770-2019 |
|---|---|
| Recall event | 82752 |
| Product | Alaris Pump Infusion Set, Model Codes 10010453, 10010454, 10012144, 10015294, 10015414, 10933805, 11171447, 11404930, 11522558, 11607704, 10013361T, 2110-0500, 2126-0500, 2200-0500, 2411-0500, 2419-0007, 2420-0007, 2420-0500, 2421-0500, 2426-0007, 2426-0500, 2429-0500, 2433-0007, 2477-0000… |
| Product code | FPA |
| Recalling firm | Becton Dickinson & Company |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jul 19, 2021 |
| 510(k) numbers | K894842 |
| FEI number | 2243072 |
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