Device recall
Z-0665-2022: BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device…
FDA device recall · Class III · Becton Dickinson & Company
Key facts
| Recall number (Z-number) | Z-0665-2022 |
|---|---|
| Recall event | 89486 |
| Product | BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a catheter port equipped with a threaded female luer during blood or urine sample collection using evacuated BD Vacutainer Blood or Urine Collection Tubes Catalog Number: 364902… |
| Product code | JKA |
| Recalling firm | Becton Dickinson & Company |
| Recall class | Class III |
| Status | Open, Classified |
| 510(k) numbers | K991088 |
| 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