Device recall
Z-0089-2012: CORFLO 300 Enteral Pump; a volumetric rotary peristaltic intermittent enteral…
FDA device recall · Class II · CORPAK MedSystems
Key facts
| Recall number (Z-number) | Z-0089-2012 |
|---|---|
| Recall event | 59969 |
| Product | CORFLO 300 Enteral Pump; a volumetric rotary peristaltic intermittent enteral feeding pump; CORPAK MedSystems, Wheeling, IL 60090; catalog/reorder #20-0500. Intended to deliver formula to patients requiring tube feedings. |
| Product code | LZH |
| Recalling firm | CORPAK MedSystems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 27, 2017 |
| 510(k) numbers | K944750 |
| FEI number | 3011270181 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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