Device recall
Z-0176-2012: BD Microtainer MAP Microtube for Automated Process with K2EDTA. For the…
FDA device recall · Class III · Becton Dickinson & Company
Key facts
| Recall number (Z-number) | Z-0176-2012 |
|---|---|
| Recall event | 59684 |
| Product | BD Microtainer MAP Microtube for Automated Process with K2EDTA. For the collection, transport, and automated processing of skin punctures samples from infants, children, geriatric, oncology, and critical care patients. |
| Product code | JKA |
| Recalling firm | Becton Dickinson & Company |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 10, 2011 |
| 510(k) numbers | K093972 |
| FEI number | 2243072 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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