Device recall
Z-2545-2020: Centurion DIFFICULT IV KIT containing BD's Vacutainer Plastic Lithium Heparin…
FDA device recall · Class II · Centurion Medical Products Corporation
Key facts
| Recall number (Z-number) | Z-2545-2020 |
|---|---|
| Recall event | 85494 |
| Product | Centurion DIFFICULT IV KIT containing BD's Vacutainer Plastic Lithium Heparin Tubes (BD Vacutainer-BD Codes 367884 & 367960; Centurion code 45177 (VACUTAINER GREEN TOP) and 84815 (VACUTAINER 3ML LT. GREEN). Centurion Kit Code: IV8860 |
| Product code | JKA |
| Recalling firm | Centurion Medical Products Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 21, 2021 |
| FEI number | 3008403546 |
At a glance
- None 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