B Braun recalls Perfusor Space Infusion Pump System (model 8713030U) due to potential incompatibility with Cardinal Health Monoject syringes, risking overdose or underdose in medical use. Affected users should check their syringe type and contact for guidance.
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 its Perfusor Space Infusion Pump System (model 8713030U) because it may not work properly with Cardinal Health Monoject syringes. This could lead to incorrect dosing, delays in treatment, or other issues for patients using the pump.
The pump may not recognize or properly interact with Cardinal Health Monoject syringes due to manufacturing changes. This can cause incorrect dosing, delays in therapy, or failure to trigger important safety alarms.
Healthcare providers and patients using the Perfusor Space Infusion Pump System with Cardinal Health Monoject syringes are most at risk. The recall affects devices sold with these specific syringes.
Check if your pump has model number 8713030U. The recall applies to devices that were sold with Cardinal Health Monoject syringes.
Verify your syringe type matches the pump's requirements; use only compatible syringes as specified by the manufacturer.
The pump may not work properly with Cardinal Health Monoject syringes due to manufacturing changes, risking incorrect dosing or treatment delays.
Check if your syringe is compatible with the pump. If unsure, contact B Braun for guidance.
Yes, using incompatible syringes could cause overdose, underdose, or delays in therapy or alarms.
We’ve drafted a message you can send B Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2433-2024 — B Braun B Braun Hello, I own a B Braun that is covered by recall Z-2433-2024 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.
