Device recall
Z-1180-2018: BD Vacutainer Barricor" Lithium Heparin Plasma Blood Collection Tubes for…
FDA device recall · Class II · Becton Dickinson & Company
Key facts
| Recall number (Z-number) | Z-1180-2018 |
|---|---|
| Recall event | 78909 |
| Product | BD Vacutainer Barricor" Lithium Heparin Plasma Blood Collection Tubes for Invitro Diagnostic Use, Catalog Numbers: 365043, 365044, 365045 & 365047 Used to collect, separate, process, transport and store venous blood samples for use in chemistry determinations, therapeutic drug monitoring and zinc… |
| Product code | JKA |
| Recalling firm | Becton Dickinson & Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 4, 2019 |
| 510(k) numbers | K160657 |
| 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