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Stop using now Food recall · FDA · Published February 13, 2026

Rosabella Moringa Capsules Recall: Salmonella Contamination Risk

Rosabella Moringa dietary supplements may contain Salmonella. Consumers should stop using affected lots from March 2027 to June 2027. Recall details and action steps provided.

🇺🇸 FDA recall #H-0546-2026FoodRosabella ›
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Recalling firmAmbrosia Brands LLC136 Madison Ave # 6f · New York, NY 10016-6711
✎ GovInfoNow plain-language explainer

What happened, in plain English

Rosabella brand Moringa dietary capsules are being recalled due to possible Salmonella contamination. This could cause food poisoning if consumed, so affected consumers should stop using the product immediately. Read more at govinfonow.com/recall/6741-rosabella-moringa-capsules-recall-salmonella-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/6741-rosabella-moringa-capsules-recall-salmonella-contamination-risk · Updated August 17, 2026 · Official notice: FDA #H-0546-2026

Cite this page

“Rosabella Moringa Capsules Recall: Salmonella Contamination Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/6741-rosabella-moringa-capsules-recall-salmonella-contamination-risk. Based on FDA recall #H-0546-2026.

Why it’s dangerous

Salmonella bacteria can cause food poisoning, leading to symptoms like diarrhea, fever, and abdominal cramps. If the contaminated capsules are ingested, these symptoms may occur, especially in vulnerable individuals.

Who’s affected

Anyone who owns or uses Rosabella Moringa capsules with the listed lot numbers (March 2027 to June 2027) is affected. People with compromised immune systems are at higher risk for serious illness.

How to tell if you have this one

Check the product label for the Rosabella brand Moringa capsules. Look for lot numbers between 5020591 and 5100048, with expiration dates from March 2027 to November 2027.

  • Brand
    Rosabella
  • Product
    Rosabella brand MORINGA; DIETARY SUPPLEMENT CAPSULES; 60 capsules per bottle; Distributed by: Ambrosia Brands, LLC, 625
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Capsules

    Immediately stop using Rosabella Moringa capsules with the listed lot numbers as they may contain Salmonella.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFLPuerto Rico: yesPR

FDA distribution: “Nationwide in the United States, including American Samoa, Northern Mariana Islands, Puerto Rico, and Virgin Islands. International distribution to consumers in: Algeria, Anguilla, Australia, Austria, Bahrain, Belgium, Bosnia and…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 6 months after the firm started it.

1. Firm started the recall: Feb 13, 202612. FDA classified it Class I: Mar 9, 202623. Published in FDA’s Enforcement Report: Mar 18, 202634. FDA terminated the recall: Aug 13, 202642026
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

What should I do if I have the affected capsules?

Stop using the capsules immediately and dispose of them safely. Do not consume the product.

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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 #H-0546-2026 (February 13, 2026)
  • Plain-language summary written by qwen3:4b on August 17, 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