Device recall
Z-2432-2019: EXACTAMED Oral Dispensers, 5mL, AMBER: PHARMACY PACK, REF H9388505, x500…
FDA device recall · Class III · Baxter Healthcare Corporation
Key facts
| Recall number (Z-number) | Z-2432-2019 |
|---|---|
| Recall event | 83230 |
| Product | EXACTAMED Oral Dispensers, 5mL, AMBER: PHARMACY PACK, REF H9388505, x500 PHARMACY PACK, REF H9388105, x100 COST CONTAINMENT, REF H93884205, x1500 |
| Product code | KYX |
| Recalling firm | Baxter Healthcare Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 2, 2020 |
| FEI number | 1417572 |
At a glance
- None 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