Official recall record
8713051U, Infusomat Large Volume Pump, Wireless; Volumetric Infusion Pump System
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2023-09-21
- Country of alert
- United States
- Alert level
- Class I
- Alert type
- recall
- Barcode (EAN/GTIN)
- 04046964660887
- Brand on record
- B. Braun Medical, Inc.
What the authority reported
Upstream occlusion alarm may sound when no occlusion exists, and the device will stop pumping. Interruption to the infusion of high-risk medications may lead to hemodynamic instability requiring medical intervention to prevent permanent impairment to body structures or body functions. In some cases, this may be life-threatening or may lead to death.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
Other recalls from this brand
- 2024-06-17 · US FDA — Medical Devices
OUTLOOK PUMP SET 3 CARESITE LADS 133 IN.-Used with an electrically-powered infusion pump for intravenous (IV) - 2024-06-17 · US FDA — Medical Devices
Infusomat SPACE PUMP IV SET, 127 IN.-Used with an electrically-powered infusion pump for intravenous (IV) adm - 2024-06-17 · US FDA — Medical Devices
Infusomat 60DROP METRISET PUMP SET, 3 SAFELINE-Used with an electrically-powered infusion pump for intravenou
All 46 official recall notices naming B. Braun Medical, Inc. on this site →
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