Device recall
Z-2331-2025: Injection needle, bayonet, Luer-Lock, 1. Model no. 50-353-23, working length 25…
FDA device recall · Class II · Spiggle & Theis Mt Gmbh
Key facts
| Recall number (Z-number) | Z-2331-2025 |
|---|---|
| Recall event | 97229 |
| Product | Injection needle, bayonet, Luer-Lock, 1. Model no. 50-353-23, working length 25 cm, total length 31cm, nonsterile; 2. Model no. 50-345-23, working length 24 cm, total length 31 cm, non-sterile |
| Product code | GDM |
| Recalling firm | Spiggle & Theis Mt Gmbh |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3002858762 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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