FDA Device recall Z-2433-2021
AMSORB PLUS PREFILLED G-CAN 1.0L
- FDA Device
- Class I
- terminated
- Published 2021-09-22
On 2021-09-22 the FDA classified a Class I recall of AMSORB PLUS PREFILLED G-CAN 1.0L by Armstrong Medical Services, citing some devices may be associated with high and unexpected resistance to gas flow during clinical use, impacting or preventing adequate ventilation of an anaesthetised patient, which….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2433-2021 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2021-08-05 |
| Published | 2021-09-22 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Armstrong Medical Services |
| Distribution | US |
Product
AMSORB PLUS PREFILLED G-CAN 1.0L; Carbon dioxide absorbent canister; Product codes AMAB3801 and AMAB3801GE. Used in anesthesia.
Reason
Some devices may be associated with high and unexpected resistance to gas flow during clinical use, impacting or preventing adequate ventilation of an anaesthetised patient, which could cause a delay in treatment. Not all defective canisters will be identified by the pre-use test.
Identifiers
| code_info | LOTS 010321F51 010421F11 010421F111 010621F11 010621F111 010920F61 010920F611 011020F21 011020F211 011220F414 020621F21…LOTS 010321F51 010421F11 010421F111 010621F11 010621F111 010920F61 010920F611 011020F21 011020F211 011220F414 020621F21 020621F211 020920F11 020920F111 020920F112 020920F113 030621F41 030621F411 030820F51 030820F511 030820F512 030820F513 040121F412 040121F413 040621F11 040621F111 040920F21 040920F211 040920F212 040920F213 050521F41 050521F411 050521F51 050521F511 050521F512 060521F21 060521F211 070521F41 070521F411 070621F31 080121F31 080121F311 080121F312 090321F111 090321F112 090321F113 090920F31 090920F311 090920F312 090920F313 091220F51 091220F511 091220F512 100321F21 100321F211 100321F212 100521F21 100521F211 100521F212 110221F111 110321F31 110321F311 110521F31 120321F41 120321F411 120421F21 120421F211 120421F212 120521F411 120521F412 130121F11 130121F111 130121F112 130421F31 130521F51 130521F511 130521F512 141220F11 141220F111 141220F112 150221F21 150221F211 150321F51 150321F511 160221F31 160221F311 160321F11 160321F111 160421F511 160920F41 160920F411 160920F412 160920F413 170321 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2433-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.