Device recall
Z-1059-2026: Medline Kits containing B. Braun IV Administration Sets and Pump Administration…
FDA device recall · Class II · Medline Industries, LP
Key facts
| Recall number (Z-number) | Z-1059-2026 |
|---|---|
| Recall event | 98154 |
| Product | Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: NEURO ANGIO PACK, Medline kit SKU DYNJ38935 |
| Product code | OJG |
| Recalling firm | Medline Industries, LP |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1417592 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 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