Device recall
Z-2544-2020: Cardinal Health NPWT Occlusion Detection Canister 300cc, Prescription Only…
FDA device recall · Class II · Cardinal Health 200, LLC
Key facts
| Recall number (Z-number) | Z-2544-2020 |
|---|---|
| Recall event | 85803 |
| Product | Cardinal Health NPWT Occlusion Detection Canister 300cc, Prescription Only - Product Usage: The systems are intended for use on patients with chronic, acute, traumatic, sub-acute and dehisced wounds, partial-thickness burns, ulcers (such as diabetic or pressure), flaps and grafts. The Cardinal… |
| Product code | OMP |
| Recalling firm | Cardinal Health 200, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 5, 2025 |
| 510(k) numbers | K143016 |
| FEI number | 3001236905 |
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