Device recall
Z-1446-06: BD Unopette -- System Tests (Erythrocyte Fragility Test Kit). Catalog # 365830…
FDA device recall · Class II · Becton Dickinson & Company
Key facts
| Recall number (Z-number) | Z-1446-06 |
|---|---|
| Recall event | 35864 |
| Product | BD Unopette -- System Tests (Erythrocyte Fragility Test Kit). Catalog # 365830, Exp Date 2006-06, Manufactured by BD in San Lorenzo, Puerto Rico. |
| Product code | GKE |
| Recalling firm | Becton Dickinson & Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 25, 2006 |
| FEI number | 2243072 |
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