Device recall
Z-0126-2020: 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-0126-2020 |
|---|---|
| Recall event | 83549 |
| Product | Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as High-Pressure Filter PRIMARY I.V. PLUMSET Convetible Pin, 104 Inch with Orange Polyethylene-Lined*/Light Resistant Tubing, Prepierced Injection Site and OPTION-LOK. 1 unit per pouch; 48… |
| Product code | FRN |
| Recalling firm | ICU Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 12, 2024 |
| 510(k) numbers | K982159 |
| FEI number | 3013319212 |
At a glance
- 1–9 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