FDA Device recall Z-3139-2024
Alaris PCA Module Model 8120, 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 PCA Module Model 8120, 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-3139-2024 |
| 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 PCA Module Model 8120, 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: 8120 UDI-DI codes: 10885403516030, 10885403515316, 10885403812033, 10885403812026, 10885403494291, 108854…Model Number: 8120 UDI-DI codes: 10885403516030, 10885403515316, 10885403812033, 10885403812026, 10885403494291, 10885403812002 Serial Numbers: 16473112 16474187 16458453 16458381 16458632 16472825 16456729 16457626 16453240 16458585 16450364 16459191 16458699 16473046 16458427 16473677 16472463 16459701 16472829 16458736 16458700 16457828 16460132 16455368 16472831 16473116 16457873 16460396 16473618 16473688 16458544 16458121 16473391 16527718 16527910 16441259 16441394 16528387 16441214 16477919 16441048 16525578 16440759 16441453 16525916 16441034 16441160 16441164 16450345 16441601 16454386 16442620 16479558 16452454 16358256 16452960 16453953 16452089 16472866 16452442 16449483 16282569 16452076 16473123 16453256 16448217 16452996 16438128 16453852 16282541 16453263 16453423 16454448 16452576 16450489 16453424 16453702 16453853 16452088 16452445 16453527 16298268 16454345 16282360 16452394 16280503 16452485 16298349 16440752 16441277 16453848 16451983 16453700 16454300 16453421 1 |
|---|
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-3139-2024%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.