CareFusion recalls Alaris Pump Model 8100 units with FR-110 plastic bezels made between April 2011 and June 2017 due to potential weakening that could cause infusion errors.
The bezel manufacturing process for the FR-110 plastic may have resulted in its weakening. A bezel with weakened plastic may, over time, lead to separation of the bezel post (recall issue) as well as other damage to the bezel (i.e. external cracking). The separation of one or more bezel posts may result in free flow, over infusion, under infusion or interruption of infusion.
CareFusion is recalling Alaris Pump Model 8100 devices with bezels made using FR-110 plastic resin from April 2011 to June 2017. Weakened plastic could cause the bezel to separate, leading to infusion errors like over or under delivery of medication.
The FR-110 plastic used in the bezel may weaken over time, causing the bezel posts to separate. This separation can lead to infusion errors such as over-infusion, under-infusion, or interruption of medication delivery.
Patients using Alaris Pump Model 8100 for IV medication delivery are most at risk. The recall affects pumps manufactured between April 2011 and June 2017 with specific bezel assemblies.
Check if your Alaris Pump Model 8100 was manufactured between April 2011 and June 2017 with bezel assemblies made using FR-110 plastic resin. Look for specific pump assembly part numbers: 10942012, 49000007, 49000203, 10964559, or 49000204.
Verify your Alaris Pump Model 8100 was manufactured between April 2011 and June 2017 with bezel assemblies using FR-110 plastic resin.
Reach out to CareFusion for specific replacement or repair options for affected pumps.
The FR-110 plastic used in the bezel may weaken over time, causing bezel posts to separate and potentially leading to infusion errors like over or under delivery of medication.
Pumps with part numbers 10942012, 49000007, 49000203, 10964559, or 49000204 are affected.
Check if your Alaris Pump Model 8100 was manufactured between April 2011 and June 2017 with bezel assemblies made using FR-110 plastic resin.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-1768-2019 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-1768-2019 from CareFusion. 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.
