Device recall
Z-2433-2021: AMSORB PLUS PREFILLED G-CAN 1.0L; Carbon dioxide absorbent canister; Product…
FDA device recall · Class I · Armstrong Medical Services Limited
Key facts
| Recall number (Z-number) | Z-2433-2021 |
|---|---|
| Recall event | 88462 |
| Product | AMSORB PLUS PREFILLED G-CAN 1.0L; Carbon dioxide absorbent canister; Product codes AMAB3801 and AMAB3801GE. Used in anesthesia. |
| Product code | CBL |
| Recalling firm | Armstrong Medical Services Limited |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Sep 17, 2024 |
| FEI number | 3002226076 |
At a glance
- None 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