Device recall
Z-0139-2020: Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets…
FDA device recall · Class II · ICU Medical Inc
Key facts
| Recall number (Z-number) | Z-0139-2020 |
|---|---|
| Recall event | 83549 |
| Product | Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as Primary PLUM Set, 15 Micron Filter in Sight Chamber, CLAVE Secondary Port, 0.2 Micron Filter, Polyethylene Lined Light Resistant Tubing, Distal Microbore Tubing, Secure Lock 269 cm / 14 mL. 1… |
| Product code | FRN |
| Recalling firm | ICU Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 12, 2024 |
| FEI number | 3013319212 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 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