CareFusion Alaris PCA Pump Model 8120: Syringe Plunger Grippers May Fail to Close

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Contact the company & request your remedy

Recalling firmCareFusion 303, Inc.10020 Pacific Mesa Blvd, N/A · San Diego, CA 92121-4386

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

CareFusion is recalling Alaris PCA Pump Model 8120 devices because the syringe plunger grippers might not close properly when the control knob is turned. This could lead to medication delivery problems if the plunger isn't held securely. Affected users should check if their pump was manufactured between May 2013 and April 2017.

Why it’s dangerous

The syringe plunger grippers may fail to automatically close around the syringe plunger when the control knob is turned. This could cause the plunger to move unexpectedly, potentially leading to medication delivery errors or improper dosing.

Who’s affected

Healthcare professionals and patients using the Alaris PCA Pump Model 8120 for medication delivery are most at risk. The recall affects devices manufactured between May 2013 and April 2017.

How to tell if you have this one

Check for the CareFusion label on the pump. The product was manufactured between May 1, 2013, and April 30, 2017. The model number is 8120.

Brand
CareFusion
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Date
Verify the pump was manufactured between May 1, 2013, and April 30, 2017.

✎ GovInfoNow

Questions people ask

What is the model number of the recalled pump?

The model number is 8120.

When was the pump manufactured?

The pump was manufactured between May 1, 2013, and April 30, 2017.

What should I do if I have this pump?

The recall does not specify a remedy, so you should check with CareFusion for further instructions.

Take action

Contact CareFusion

We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0323-2018 — CareFusion CareFusion

Hello,

I own a CareFusion that is covered by recall Z-0323-2018 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.

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Where this comes from

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.

Official source: FDA Recall #Z-0323-2018 (November 17, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0323-2018 to see it in context.
Plain-language summary written by qwen3:4b on September 1, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

CareFusion 303, Inc. recalls Alaris PCA Pump, Model 8120. The firm name on the label is CareFusion. The Alaris Syringe Pump module and Alaris PCA

Use caution until it’s fixed