FDA Device recall Z-3142-2024
Alaris Pump Module Model 8100, 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 Pump Module Model 8100, 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-3142-2024 |
| 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 Pump Module Model 8100, 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: 8100 UDI-DI code: 10885403810046, 10885403810039, 10885403810015 Serial Numbers: 16448779 16451711 164512…Model Number: 8100 UDI-DI code: 10885403810046, 10885403810039, 10885403810015 Serial Numbers: 16448779 16451711 16451209 16450973 16450971 16451760 16407678 16411676 16388896 16405467 16408857 16387206 16405786 16407463 16410819 16407769 16399159 16410420 16411470 16409931 16409006 16411571 16409107 16388799 16472492 16409660 16410466 16404846 16409933 16410968 16406453 16406013 16408309 16402653 16410415 16411500 16411069 16407539 16410537 16451801 16450922 16451705 16448898 16451601 16448918 16450847 16453708 16451857 16451608 16451642 16372116 16451808 16451067 16451690 16451895 16445957 16453760 16451083 16453750 16448376 16450498 16451078 16448899 16451051 16453718 16450801 16449025 16450557 16453778 16448576 16450674 16451410 16448921 16451745 16451356 16451907 16453721 16451788 16450769 16451819 16448338 16449113 16451236 16450609 16450928 16448781 16451823 16450969 16451794 16451840 16451856 16445998 16451321 16451787 16444660 16407683 16410698 16410619 16403032 16472342 16408 |
|---|
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-3142-2024%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.