Device recall
Z-0444-2026: Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits…
FDA device recall · Class I · Medline Industries, LP
Key facts
| Recall number (Z-number) | Z-0444-2026 |
|---|---|
| Recall event | 97882 |
| Product | Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; OPEN HEART SUPPLEMENT DYNJ909116D; VASCULAR DYNJ909124F |
| Product code | OEZ |
| Recalling firm | Medline Industries, LP |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 1417592 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 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