FDA Device recall Z-3140-2024
Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system
- FDA Device
- Class II
- ongoing
- Published 2024-09-25
On 2024-09-25 the FDA classified a Class II recall of Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system by Carefusion 303, citing due to affected devices that may have bent female IUI connector and may not be operable and potentially cause delays in the start of the infusion or monitoring.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3140-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-08-15 |
| Published | 2024-09-25 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system
Reason
Due to affected devices that may have bent female IUI connector and may not be operable and potentially cause delays in the start of the infusion or monitoring.
Identifiers
| code_info | Model Number: 8300 UDI-DI codes: 10885403830020, 10885403830013 Serial Numbers: 16233040 16233078 16233149 16233080 162…Model Number: 8300 UDI-DI codes: 10885403830020, 10885403830013 Serial Numbers: 16233040 16233078 16233149 16233080 16233328 16233293 16233308 16233153 16233320 16192058 16233232 16233330 16226112 16196835 16233159 16233363 16233362 16233226 16233163 16233069 16233074 16233077 16226102 16226107 16196802 16226103 16226099 16226113 16233296 16233101 16233211 16233223 16233203 16233302 16233360 16233359 16226098 16226109 16226106 16233361 16233285 16233141 16226110 16233145 16226105 16196832 16196755 16196594 16194385 16191983 16196603 16196615 16192142 16194384 16191988 16193961 16193955 16193991 16191985 16192001 16191939 16192287 16192936 16191995 16194400 16194370 16192010 16196608 16192493 16191991 16192008 16192002 16191976 16191998 16191993 16192012 16192966 16191971 16194376 16196806 16194399 16192927 16191911 16192004 16192006 16191997 16191979 16192967 16196596 16192094 16192724 16196818 16192728 16192758 16192862 16192720 16192804 16192850 16192789 16196591 16196612 16196599 16 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3140-2024%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.