CareFusion recalls Alaris Syringe Pump Model 8110 due to risk of plunger grippers failing to close, potentially causing medication delivery issues. Affected units manufactured between May 2013 and April 2017.
The syringe plunger grippers may fail to automatically close around the syringe plunger press when the gripper control knob has been closed.
CareFusion is recalling Alaris Syringe Pump Model 8110 devices because the plunger grippers might not automatically close around the syringe plunger when the control knob is closed. This could lead to medication delivery problems if the pump continues to run without the plunger being properly secured.
The syringe plunger grippers may fail to automatically close around the syringe plunger when the gripper control knob is closed. This could cause the pump to continue running without the plunger being properly secured, potentially leading to medication delivery issues.
Adults, pediatrics, and neonates using the Alaris Syringe Pump Model 8110 for medication delivery. Patients receiving continuous or intermittent medication through intravenous, subcutaneous, or epidural routes are most at risk.
Check for the Alaris Syringe Pump Model 8110 with the manufacturer name CareFusion on the label. Devices manufactured between May 1, 2013, and April 30, 2017, are affected.
Look for the Alaris Syringe Pump Model 8110 with CareFusion on the label.
The syringe plunger grippers may fail to automatically close around the syringe plunger when the gripper control knob is closed, potentially causing medication delivery issues.
Devices were manufactured between May 1, 2013, and April 30, 2017.
The recall record does not specify a remedy.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-0322-2018 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-0322-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
