Device recall
Z-0161-2013: Medpro Elastomeric Infusion Pump. AccuFlux, Model # CT-0020-100H. Product Usage…
FDA device recall · Class I · First Medical Source LLC
Key facts
| Recall number (Z-number) | Z-0161-2013 |
|---|---|
| Recall event | 60030 |
| Product | Medpro Elastomeric Infusion Pump. AccuFlux, Model # CT-0020-100H. Product Usage: The devices are intended for patients requiring intravenous, percutaneous, subcutaneous, intra-operative sites or epidural administration of medications. It is the responsibility of the user to ensure that the… |
| Product code | MEB |
| Recalling firm | First Medical Source LLC |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Sep 22, 2014 |
| 510(k) numbers | K081905 |
| FEI number | 3007008418 |
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