Device recall
Z-0455-05: BD ProbeTec ET Urine Processing Kit, 4x25, catalog 440454, packaged in a carton…
FDA device recall · Class I · Becton Dickinson & Co.
Key facts
| Recall number (Z-number) | Z-0455-05 |
|---|---|
| Recall event | 30844 |
| Product | BD ProbeTec ET Urine Processing Kit, 4x25, catalog 440454, packaged in a carton containing 4 storage bags identified as BD ProbeTec ET Urine Processing Pouches, 25 pouches/bag. Carton and bags labeled in part ***Becton, Dickinson and Company, 7 Loveton Circle, Sparks, MD 21152*** |
| Product code | LSL |
| Recalling firm | Becton Dickinson & Co. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Apr 19, 2005 |
| FEI number | 1119779 |
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