Device recall
Z-1591-2023: Vapor-Clean, Part Number 111AU The Vapor-Clean filter is intended to be used to…
FDA device recall · Class II · Dynasthetics LLC
Key facts
| Recall number (Z-number) | Z-1591-2023 |
|---|---|
| Recall event | 92026 |
| Product | Vapor-Clean, Part Number 111AU The Vapor-Clean filter is intended to be used to remove unwanted anesthetic gases from the patient breathing circuit. The device uses two anesthetic vapor adsorbent canisters connected to an anesthesia delivery system to prevent unwanted anesthetic vapors emanating… |
| Product code | CBN |
| Recalling firm | Dynasthetics LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K092031 |
| FEI number | 3008776780 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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