Becton Dickinson recalls CareFusion MaxPlus Clear Needleless Connectors due to risk of blood loss and air embolism if valve remains open after disconnection, especially in neonates. Affected units have specific lot numbers and expiration dates.
After disconnection of a luer, the valve of the connector remains recessed; not fully closing, either temporarily or permanently. The risks of blood loss and air embolism exist if the valve remains permanently open and goes undetected, especially in the neonate population.
Becton Dickinson is recalling CareFusion MaxPlus Clear Needleless Connectors because a valve may not close properly after disconnection, leading to blood loss or air embolism, particularly in newborns. This issue affects specific units with known lot numbers and expiration dates.
After disconnecting a luer fitting, the valve may stay partially open, allowing blood to leak out or air to enter the bloodstream. This can cause blood loss or air embolism, which is especially dangerous for newborns whose bodies are more sensitive to such issues.
Healthcare providers using the connector for IV therapy, especially neonatal care teams. Newborns are at higher risk due to the potential for undetected valve issues.
Check for the model number MP1000-C and lot number 18085990 on the connector. The expiration date is August 15, 2023. This recall applies to units sold with these specific identifiers.
Look for the model number MP1000-C and lot number 18085990 on the connector.
Reach out to Becton Dickinson for further assistance or to confirm if your connector is affected.
The valve may not close properly after disconnection, leading to blood loss or air embolism, especially in newborns.
Check for the model number MP1000-C and lot number 18085990. Contact Becton Dickinson for further assistance.
Yes, newborns are at higher risk due to the potential for undetected valve issues causing blood loss or air embolism.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-0049-2020 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-0049-2020 from Becton Dickinson. 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.
