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Drug recall · FDA · Published March 7, 2019

Medtech Products, Inc. recalls Little Remedies New Baby Essentials Kit. Each kit contains 1 each of the following products: Little Remedies Infant

Medtech Products recalls Little Remedies New Baby Essentials Kit due to incorrect labeling of two items. Consumers should check kit lot numbers and contact the company for details.

🇺🇸 FDA recall #D-1012-2019DrugLittle Remedies ›
Take action

Contact the company & request your remedy

Recalling firmMedtech Products, Inc.660 White Plains Rd Ste 250, N/A · Tarrytown, NY 10591-5171
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

Medtech Products is recalling Little Remedies New Baby Essentials Kits because the carton incorrectly labels two of the five products inside. This could lead to using the wrong product, which might cause harm to babies. Read more at govinfonow.com/recall/39122-little-remedies-new-baby-essentials-kit-recall-incorrect-labeling-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/39122-little-remedies-new-baby-essentials-kit-recall-incorrect-labeling-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1012-2019

Cite this page

“Little Remedies New Baby Essentials Kit Recall: Incorrect Labeling Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/39122-little-remedies-new-baby-essentials-kit-recall-incorrect-labeling-risk. Based on FDA recall #D-1012-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1012-2019%22&limit=1).

Why it’s dangerous

The kit's carton has incorrect labeling for two products, which means parents might use the wrong product by mistake. This could lead to incorrect dosing or using a product that's not safe for babies.

Who’s affected

Parents or caregivers who purchased the Little Remedies New Baby Essentials Kit with lot numbers 8473AG or 8473AI (expired 08/2020) are affected. Babies using the kit are at the highest risk.

How to tell if you have this one

Check the kit's lot number on the carton, which should be 8473AG or 8473AI. The kit was distributed by Medtech Products Inc. and expired by August 2020.

  • Brand
    Little Remedies
  • Product
    Little Remedies New Baby Essentials Kit. Each kit contains 1 each of the following products: Little Remedies Infant
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Kit Lot Number

    Look for lot numbers 8473AG or 8473AI on the carton to identify affected kits.

  2. Contact Manufacturer

    Reach out to Medtech Products Inc. for further instructions on the recall.

✎ GovInfoNow

Questions people ask

Why is this kit being recalled?

The kit's carton incorrectly labels two of the five products inside, which could lead to using the wrong product.

What products are in the kit?

The kit contains Little Remedies Infant Fever Reducer, Saline Spray/Drops, Gripe Water, Gas Relief Drops, and Boudreaux's Butt Paste.

How can I tell if I have the recalled kit?

Check the carton for lot numbers 8473AG or 8473AI, which were distributed by Medtech Products Inc. and expired by August 2020.

Take action

Contact Little Remedies

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

Subject: Recall D-1012-2019 — Little Remedies Little Remedies New Baby Essentials Kit. Each kit contains 1 each of the following 

Hello,

I own a Little Remedies New Baby Essentials Kit. Each kit contains 1 each of the following products: Little Remedies Infant that is covered by recall D-1012-2019 from Little Remedies.

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 #D-1012-2019 (March 7, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1012-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA