Device recall
Z-2424-2024: BD Nano 2nd Gen Pen Needles 32G X 4mm (5-count sample contained in Patient…
FDA device recall · Class II · Embecta Corp.
Key facts
| Recall number (Z-number) | Z-2424-2024 |
|---|---|
| Recall event | 94851 |
| Product | BD Nano 2nd Gen Pen Needles 32G X 4mm (5-count sample contained in Patient Counseling Sample Toolbox -Catalog 6484755/Lot Number: 3750144)-Sterile, single use devices designed for the parenteral administration of a drug from a cartridge contained in a drug pen injector Model/Catalog Number: 320551 |
| Product code | FMI |
| Recalling firm | Embecta Corp. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K212015 |
| FEI number | 3022699058 |
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