Device recall
Z-0360-2024: AVANOS BALLARD Closed Suction System for Adults, 14 Fr, DSE, MDI, Product code…
FDA device recall · Class II · Avanos Medical, Inc.
Key facts
| Recall number (Z-number) | Z-0360-2024 |
|---|---|
| Recall event | 93305 |
| Product | AVANOS BALLARD Closed Suction System for Adults, 14 Fr, DSE, MDI, Product code 221038, provide suction on patients on mechanical ventilation |
| Product code | BSY |
| Recalling firm | Avanos Medical, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3011270181 |
At a glance
- None 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