Device recall
Z-0148-2024: Monoject 20 mL Syringe Luer-Lock Tip Soft Pack
FDA device recall · Class I · Cardinal Health 200, LLC
Key facts
| Recall number (Z-number) | Z-0148-2024 |
|---|---|
| Recall event | 93075 |
| Product | Monoject 20 mL Syringe Luer-Lock Tip Soft Pack |
| Product code | FMF |
| Recalling firm | Cardinal Health 200, LLC |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K113091 |
| FEI number | 3001236905 |
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