Device recall
Z-2276-2026: Spinal Needle procedure kits: Material Description (Material Number) 24GA…
FDA device recall · Class I · B Braun Medical Inc
Key facts
| Recall number (Z-number) | Z-2276-2026 |
|---|---|
| Recall event | 98838 |
| Product | Spinal Needle procedure kits: Material Description (Material Number) 24GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333867); 25GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333862); GOVP24BK 24G PENCAN TRAY W/ BUP & DEXTROS (332607); P24BK 24G PENCAN TRAY W/BUP & DEXTROSE (333868); P25BKAY PENCAN SPINAL TRAY… |
| Product code | OFU |
| Recalling firm | B Braun Medical Inc |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 2521402 |
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