Device recall
Z-1023-2010: BD Vacutainer Urine Cup Kit with C&S Preservative Tube for Midstream specimens…
FDA device recall · Class III · Becton Dickinson & Company
Key facts
| Recall number (Z-number) | Z-1023-2010 |
|---|---|
| Recall event | 53650 |
| Product | BD Vacutainer Urine Cup Kit with C&S Preservative Tube for Midstream specimens; 50; Becton Dickinson and Company, Franklin Lakes, NJ 07417; Kit contains Sterile Screw-Cap collection cup with Integrated Transfer Device and 4.0 mL 13x75mm Plus Plastic C&S Preservative Tube and Castile Soap Towelettes. |
| 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