Device recall
Z-1522-2022: INTERA 3000 Hepatic Artery Infusion Pump, 30 mL, Sterile, Rx Only. implantable…
FDA device recall · Class I · Intera Oncology, Inc.
Key facts
| Recall number (Z-number) | Z-1522-2022 |
|---|---|
| Recall event | 90642 |
| Product | INTERA 3000 Hepatic Artery Infusion Pump, 30 mL, Sterile, Rx Only. implantable infusion pump. |
| Product code | LKK |
| Recalling firm | Intera Oncology, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Sep 12, 2023 |
| PMA numbers | P890055 |
| FEI number | 3015537318 |
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