Baxter ELI 380 Electrocardiograph Recall: Mistaken Shipment to Customer

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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 recalled a single ELI 380 Electrocardiograph model that was mistakenly shipped to a customer in October 2022. This was a one-time error and no action is required for the affected unit.

Why it’s dangerous

The hazard was a one-time shipping error where a specific model was sent to a customer by mistake. There is no risk of injury or malfunction as it was not intended for use.

Who’s affected

Customers who received the ELI 380 Electrocardiograph model with lot number 122420001706 in October 2022. This was a single unit shipped by mistake.

How to tell if you have this one

Check for the ELI 380 Electrocardiograph model with lot number 122420001706. This unit was shipped in October 2022 as part of a pilot program error.

Brand
Baxter
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Your Unit
Verify if your ELI 380 Electrocardiograph has lot number 122420001706 and was shipped in October 2022.

✎ GovInfoNow

Questions people ask

Is this product dangerous?

No, this was a one-time shipping error and the unit was not intended for use. No action is needed.

Do I need to do anything with this unit?

No action is required as this was a single unit shipped by mistake and not intended for use.

What is the lot number for this recalled unit?

The lot number is 122420001706.

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-1013-2023 — Baxter Baxter

Hello,

I own a Baxter that is covered by recall Z-1013-2023 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.

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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-1013-2023 (October 31, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1013-2023 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 Baxter Electrocardiograph, ELI 380 -DCS21

Lower-risk recall