FDA Medical Device Recalls (openFDA)
B Braun Medical Inc: Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U
- Recall number
- Z-2972-2024
- Recalling firm
- B Braun Medical Inc
- Product
- Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U
- Status
- Open, Classified
- Initiated
- 2024-08-07
- Posted
- 2024-09-07
- Terminated
- not on file
- 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.
- Root cause
- Component design/selection
- Action
- On August 7, 2024, the firm notified customers via "URGENT MEDICAL DEVICE CORRECTION" letters which specified that previous recall RES 92978 had been extended to include additional serial numbers as well as one additional model number. The updated serial numbers for the prior models has been documented under RES 92978. This present record documents the addition of model number 8713050U. Customers were instructed to identify affected units in their facilities and to place the provided stickers on impacted units to aid clinical and biomedical staff in identifying units which require sensor exchange and application of interim control measures described in the letter. The firm recommends that consignees use non-impacted devices for the delivery of high-risk medications, and do not use impacted serial numbers for high-risk medications until the upstream occlusion sensor can be replaced. Return the product correction acknowledgement for to B.Braun Medical Inc. Quality Assurance department by faxing the form to (610) 849-1197 or e-mail to PA_QualityAssurance.BBMUS_Service@bbraunusa.com even if the total inventory in your possession is zero (0). A Field Service Representative will contact customers to arrange for a time and date to check their pump and replace their impacted sensors. If you have any questions, contact us at 610-266-0500.
- Quantity
- 14
- Distribution
- US distribution to AL, CA, GA, IL, MI, and TX.
- Lot, serial or model codes
- UDI-DI (GUDID) - 04046963716752 Serial Numbers 52226, 107529, 123259, 123815, 123843, 139003, 147678, 147721, 147725, 239018, 239165, 239231, 239279, 339337
- 510(k) numbers
- K191910
- PMA numbers
- not on file
- Product code
- FRN
- Firm FEI
- 3003218564
- Firm city
- Breinigsville
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28