Device recall
Z-0009-2013: Wound Pro Apex Negative Pressure Wound Therapy Powered Suction Pump; Accuro…
FDA device recall · Class II · Accuro Medical Product LLC
Key facts
| Recall number (Z-number) | Z-0009-2013 |
|---|---|
| Recall event | 63064 |
| Product | Wound Pro Apex Negative Pressure Wound Therapy Powered Suction Pump; Accuro Medical Products LLC, 2854 Hitchcock Ave, Downers Grove, IL 60515; part number 84635400182, sold inside the Apex Negative Wound Therapy system, part number 84635400181 Promotes wound healing through drainage and removal of… |
| Product code | OMP |
| Recalling firm | Accuro Medical Product LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 27, 2017 |
| 510(k) numbers | K100823 |
| FEI number | 3007793449 |
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