FDA Device recall Z-2972-2024
Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U
- FDA Device
- Class I
- ongoing
- Published 2024-09-18
On 2024-09-18 the FDA classified a Class I recall of Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U by B Braun Medical, citing extension of previous recall RES 92978. Pumps have the potential for upstream occlusion sensor to cease proper function due to buildup of electrostatic charge during operation tri….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2972-2024 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2024-08-07 |
| Published | 2024-09-18 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | B Braun Medical |
| Distribution | AL, CA, GA, IL, MI, TX |
Product
Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U
Reason
Extension of previous recall RES 92978. Pumps have the potential for upstream occlusion sensor to cease proper function due to buildup of electrostatic charge during operation triggering false downstream and upstream occlusion alarms. Additional devices have been affected.
Identifiers
| code_info | UDI-DI (GUDID) - 04046963716752 Serial Numbers 52226, 107529, 123259, 123815, 123843, 139003, 147678, 147721, 147725, 239018, 239165, 239231, 239279, 339337 |
|---|
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-2972-2024%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.