Device recall
Z-2296-2026: Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used…
FDA device recall · Class II · Bayer Medical Care, Inc.
Key facts
| Recall number (Z-number) | Z-2296-2026 |
|---|---|
| Recall event | 98881 |
| Product | Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad Avanta Injection System; Catalog number: AVA 500 MPAT (Part 2 of 2); Affected material numbers: 87629007, 60729458, 86566648; |
| Product code | DXT |
| Recalling firm | Bayer Medical Care, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K050456 |
| FEI number | 2520313 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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