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# Braun Medical Expands Infusion Pump Recall
- URL: https://www.fdaweb.com/braun-medical-expands-infusion-pump-recall/
- Published: 2024-09-18T12:00:00.000Z
- Updated: 2026-09-14T14:41:42.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5157800

Braun Medical is expanding an [earlier recall](https://www.fda.gov/medical-devices/medical-device-recalls/b-braun-medical-inc-recalls-infusomat-space-large-volume-pump-wireless-and-infusomat-space-large?ref=fdaweb.com) to add lnfusomat Space Infusion System/Large Volume Pump to previous recalled devices — Infusomat Space Large Volume Pump Wireless, and lnfusomat Space Large Volume Pump Non-Wireless Battery Pack — due to the risk that an alarm may sound to indicate an occlusion when no blockage is present. The erroneous alarm can cause the pumps to stop delivering medications, according to a [recall notice](https://www.fda.gov/medical-devices/medical-device-recalls/infusion-pump-correction-b-braun-medical-inc-issues-correction-lnfusomat-space-infusion-systemlarge?ref=fdaweb.com). “The use of affected product may cause serious adverse health consequences, including abnormal or unstable blood pressure (hemodynamic instability) and death,” it says. To date, there has been one reported injury and one death report.  
  
FDA notes that the recall involves correcting the devices and not removing them from the market, the notice says, adding that B. Braun Medical is working to schedule and update affected devices.  
  
 Braun Medical expands an [earlier recall](https://www.fda.gov/medical-devices/medical-device-recalls/b-braun-medical-inc-recalls-infusomat-space-large-volume-pump-wireless-and-infusomat-space-large?ref=fdaweb.com) to add lnfusomat Space Infusion System/Large Volume Pump to previous recalled devices due to an erroneous alarm that may sound and interrupt therapy.