B Braun recalls Perfusor Space syringe pumps with model 8713080U due to potential incompatibility with Cardinal Health Monoject syringes, risking overdose or underdose in medical use. Affected units may need replacement to ensure safe therapy delivery.
Perfusor Space Syringe Pump's instructions for use previously identified Monoject syringes as an option for use. However, changes to manufacturing to Cardinal Health Monoject syringes may result in issues with recognition, compatibility, and pump performance, such as overdose, underdose, delay in therapy, delay in occlusion alarms, and delay in feeding. Cardinal Health Monoject syringes are not compatible with the indicated pumps.
B Braun is recalling Perfusor Space syringe pumps (model 8713080U) because they may not work properly with Cardinal Health Monoject syringes, which could lead to incorrect medication dosing. This is a serious risk for patients using these pumps for medical treatments.
The Perfusor Space pump was designed to work with specific syringes, but changes in manufacturing of Cardinal Health Monoject syringes may cause the pump to misread the syringe. This could lead to incorrect medication doses, such as overdose or underdose, delaying critical therapy or alarms.
Healthcare professionals using the Perfusor Space syringe pump with Cardinal Health Monoject syringes are most at risk. Patients receiving medical therapy through this pump could experience incorrect dosing if the syringe is incompatible.
Check for the model number 8713080U on the pump. The product was sold with Cardinal Health Monoject syringes, which may not be compatible with this pump.
Verify if the pump works with Cardinal Health Monoject syringes by testing the pump's response to the syringe.
The recall occurs because changes in Cardinal Health Monoject syringes may cause the Perfusor Space pump to misread the syringe, risking incorrect medication dosing.
No, but you should check if the pump works with your syringes to avoid incorrect dosing.
The official recall does not specify a remedy, so contact B Braun for guidance on safe alternatives.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2435-2024 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-2435-2024 from B Braun. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
