Device recall
Z-0147-2022: Kit: Central Line Dres Change 20/Cs
FDA device recall · Class II · Medical Action Industries, Inc. 306
Key facts
| Recall number (Z-number) | Z-0147-2022 |
|---|---|
| Recall event | 88687 |
| Product | Kit: Central Line Dres Change 20/Cs |
| Product code | PEZ |
| Recalling firm | Medical Action Industries, Inc. 306 |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 13, 2023 |
| FEI number | 1030451 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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