Device recall
Z-0178-2015: Cardiopulmonary bypass connector; P/N: 321334-000 DESC: CONNECTOR, 3/8 X 3/8 X…
FDA device recall · Class II · Dokitz NovoSci
Key facts
| Recall number (Z-number) | Z-0178-2015 |
|---|---|
| Recall event | 69535 |
| Product | Cardiopulmonary bypass connector; P/N: 321334-000 DESC: CONNECTOR, 3/8 X 3/8 X 1/2 CLEAR PAY LOT: 295424 STERILE Expiration May 2019 Manufacturing Date May 2014 |
| Product code | DTL |
| Recalling firm | Dokitz NovoSci |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 15, 2015 |
| 510(k) numbers | K801404 |
| FEI number | 1625519 |
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