Device recall
Z-2790-2016: Hospira MedNet Medication Management Suite software, version 6.1, List Numbers…
FDA device recall · Class II · Hospira Inc., A Pfizer Company
Key facts
| Recall number (Z-number) | Z-2790-2016 |
|---|---|
| Recall event | 74903 |
| Product | Hospira MedNet Medication Management Suite software, version 6.1, List Numbers 16037-64-02 and 16037-64-03, in combination with the SapphirePlus 13.1x infusion pump Hospira MedNet Medication Management Suite is intended to facilitate networked communication between compatible computer systems and… |
| Product code | FRN |
| Recalling firm | Hospira Inc., A Pfizer Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 2, 2018 |
| 510(k) numbers | K141102 |
| FEI number | 3013319212 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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