Device recall
Z-3044-2026: Halyard medical convenience kits labeled as: 1) ENT, Model/Item Number (kit)…
FDA device recall · Class II · AVID Medical, Inc.
Key facts
| Recall number (Z-number) | Z-3044-2026 |
|---|---|
| Recall event | 99469 |
| Product | Halyard medical convenience kits labeled as: 1) ENT, Model/Item Number (kit) ACEN89-01; 2) ENT, Model/Item Number (kit) ACEN89-02; 3) BACK PACK, Model/Item Number (kit) ALBK51-01; 4) DR DERIAN SPINE PACK SNEDHCPDH, Model/Item Number (kit) DGSP71; 5) BASIC PACK DR BROWN SBADHBPR16, Model/Item Number… |
| Product code | LRO |
| Recalling firm | AVID Medical, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1047429 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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