Infusomat recallZ-2972-2024 · B Braun Medical Inc · initiated Aug 7, 2024
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from B Braun Medical Inc or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
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.
FDA root cause category: Component design/selection
What the company is doing
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 [email protected] 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.
Recall details
- Recall number
- Z-2972-2024
- Status
- Open, Classified
- Initiated by the company
- Aug 7, 2024
- Posted by the FDA
- Sep 7, 2024
- Recalling firm
- B Braun Medical Inc
- Quantity
- 14
- Product code
- FRN
- FDA submissions
- K191910
- Distribution
- US distribution to AL, CA, GA, IL, MI, and TX.
Product description
Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U
Code information (models, lots, serial numbers)
UDI-DI (GUDID) - 04046963716752 Serial Numbers 52226, 107529, 123259, 123815, 123843, 139003, 147678, 147721, 147725, 239018, 239165, 239231, 239279, 339337
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- Infusomat® 8713050UB. Braun Medical Inc. · Pump, infusion1 recall2 deaths136 reports
Product lines
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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