Device recall
Z-0779-2020: Medical convenience trays and kits, labeled as: Medical Action Industries, Inc…
FDA device recall · Class II · Medical Action Industries, Inc. 306
Key facts
| Recall number (Z-number) | Z-0779-2020 |
|---|---|
| Recall event | 84435 |
| Product | Medical convenience trays and kits, labeled as: Medical Action Industries, Inc.: ***CVC*** Clear Sequence Change Kit, REF 77070B ***DIALYSIS*** Clear Sequence Change Kit, REF 77068B ***PEDS CVC*** Clear Sequence Change Kit, REF 77190B ***PICC*** Clear Sequence Change Kit, REF 77069B Adult Central… |
| Product code | KDD |
| Recalling firm | Medical Action Industries, Inc. 306 |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 24, 2023 |
| FEI number | 1030451 |
At a glance
- None 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