FDA-Device2024-09-18Class I
Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U
Hazard
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.
Sold states
US distribution to AL, CA, GA, IL, MI, and TX.
Affected count
14
Manufactured in
200 Boulder Dr, Breinigsville, PA, United States
Products
Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2972-2024More B Braun Medical Inc recalls
- FDA-Device2026-04-22B. Braun StreamLine Bloodline hemodialysis tubing recalled for air bubble accumulation risk
- FDA-Device2026-04-22B. Braun STREAMLINE BLOODLINE SET recalled for air bubble risk in hemodialysis
- FDA-Device2026-04-22B. Braun Hemodialysis Bloodlines, STREAMLINE FRESENIUS FOR DAVITA. Model Number: SL-2000M2095DA.
- FDA-Device2026-04-22B Braun hemodialysis bloodlines recalled for potential air bubble accumulation in arterial line
- FDA-Device2026-04-22B. Braun hemodialysis bloodlines recalled for potential air bubble accumulation
Don't want to check this manually?
We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.
Get the Sunday Brief