Baxter Prismaflex System Recall: Proper Connector Use Safety

Take action

Contact the company & request your remedy

Recalling firmBaxter Healthcare Corporation1 Baxter Pkwy, N/A · Deerfield, IL 60015-4625

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

Baxter is recalling its Prismaflex System and Control Unit products. This recall is based on safety information from the operator's manual about proper connector use.

Why it’s dangerous

The recall involves safety information from the operator's manual about proper connector use. This suggests potential risks if connectors are not used correctly, though the specific hazard is not detailed in the recall notice.

Who’s affected

Users of the Prismaflex System and Control Unit are affected. Healthcare professionals using these products for medical purposes are most at risk.

How to tell if you have this one

Check for the Prismaflex System and Control Unit with Product Code 113081 or GTIN 07332414105266. These products were sold by Baxter Healthcare Corporation.

Brand
Baxter
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Review Operator's Manual
Check the Prismaflex Operator's Manual for proper connector usage instructions.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

Baxter is communicating safety information from the Prismaflex Operator's Manual regarding proper connector use.

What should I do if I have this product?

The recall does not specify a remedy, so no action is required beyond reviewing the operator's manual for proper connector use.

Is there a risk of injury from this product?

The recall does not describe a specific hazard mechanism, so the risk is low based on the information provided.

Take action

Contact Baxter

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

✉️ Open in email

Subject: Recall Z-1829-2020 — Baxter Baxter

Hello,

I own a Baxter that is covered by recall Z-1829-2020 from Baxter.

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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-1829-2020 (February 6, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1829-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.

Baxter Healthcare Corporation recalls Prismaflex System, Prismaflex Control Unit

Lower-risk recall