Baxter Prismaflex System Recall: Proper Connector Use Safety

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

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Baxter Healthcare is recalling its Prismaflex System and Control Units because the operator's manual contains safety information about proper connector use. This recall is about ensuring safe operation of the medical device, not an immediate safety hazard.

Why it’s dangerous

The hazard involves potential safety risks if connectors are not used correctly according to the operator's manual. This could lead to improper device function or safety issues during medical procedures.

Who’s affected

Users of the Prismaflex System and Control Units for medical applications are affected. Healthcare professionals using these devices are most at risk if they don't follow the safety information in the operator's manual.

How to tell if you have this one

Check for the product code 955792 or GTIN 07332414126766 on the Prismaflex System and Control Units. The recall applies to devices sold by Baxter Healthcare.

Brand
Baxter Healthcare
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 safety information on connector use.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

Baxter Healthcare is communicating safety information from the Prismaflex Operator's Manual regarding proper connector use to ensure safe operation of the system.

Is there a risk of injury from this product?

The recall is about ensuring safe operation through proper connector use; there is no stated risk of injury in normal use.

How do I know if I have the recalled product?

Look for product code 955792 or GTIN 07332414126766 on the Prismaflex System and Control Units.

Take action

Contact Baxter Healthcare

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

✉️ Open in email

Subject: Recall Z-1833-2020 — Baxter Healthcare Baxter Healthcare

Hello,

I own a Baxter Healthcare that is covered by recall Z-1833-2020 from Baxter Healthcare.

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-1833-2020 (February 6, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1833-2020 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