Device recall
Z-1025-2010: BD Vacutainer Urine Complete Kit with UA Preservative Tube and C&S Preservative…
FDA device recall · Class III · Becton Dickinson & Company
Key facts
| Recall number (Z-number) | Z-1025-2010 |
|---|---|
| Recall event | 53650 |
| Product | BD Vacutainer Urine Complete Kit with UA Preservative Tube and C&S Preservative Tube for Midstream Specimens PLUS Plastic, Sterile Cup and Tube Interiors. Store at 4-25 degrees C. For In Vitro Diagnostic Use. Becton Dickinson and Company, Franklin Lakes, NJ. |
| Product code | JSM |
| Recalling firm | Becton Dickinson & Company |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 10, 2010 |
| 510(k) numbers | K024240 |
| FEI number | 2243072 |
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