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FDA recall, , High risk

Rosabella Brand Moringa Dietary Supplement Capsules

Rosabella Moringa capsules may be contaminated with Salmonella, which can cause serious infections.

Recall ended Aug 13, 2026. Still check yours.

What happened

Ambrosia Brands LLC, of New York, New York, recalled Rosabella brand MORINGA dietary supplement capsules, 60 capsules per bottle, on February 13, 2026, because the product may be contaminated with Salmonella. The company announced the recall on February 13, 2026, and the FDA added it to the Enforcement Report on March 9, 2026.

The product was distributed nationwide in the United States, including American Samoa, Northern Mariana Islands, Puerto Rico, and Virgin Islands, and internationally to consumers in many listed locations. The recall involved 1,224,208 units. The product's suggested use is to take two veggie capsules once a day with water.

2 photos

What to do

If a code on your package is listed below:

  1. Customers who have purchased the lots above are asked to dispose of it immediately, do not eat, sell, or serve the product.
  2. Consumers with questions may contact the company M-F from 9am-4pm CT at 914-768-1357.

Is yours affected?

Affected if its UPC matches.

A UPC is the number printed under a barcode.

  1. Rosabella Brand MORINGA; Dietary Supplement Capsules

    UPC
    • 8 60012 16172 0

Recall details

Company began the recall
Sold in

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 Herzegovina, Brazil, Brunei, Bulgaria, Canada, Chile, Colombia, Croatia, Cyprus, Czech Republic, Denmark, Djibouti, Dominican Republic, Egypt, Estonia, Faroe Islands, Finland, France, French Polynesia, Georgia, Germany, Gibraltar, Greece, Hong Kong, Hungary, Iceland, India, Indonesia, Ireland, Israel, Italy, Japan, Jordan, Kuwait, Latvia, Lithuania, Luxembourg, Malaysia, Malta, Marshall Islands, Mexico, Nauru, New Zealand, Netherlands, Norway, Oman, Pakistan, Peru, Philippines, Poland, Portugal, Qatar, Romania, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, South Korea, Spain, Suriname, Sweden, Switzerland, Taiwan, Thailand, Trinidad and Tobago, Turkey, United Arab Emirates, United Kingdom, Venezuela, and Zimbabwe.

Company
Ambrosia Brands LLCNew York, New York
Risk

High risk

There is a reasonable chance that eating it could cause serious health problems or death.

FDA Class I recall · How risk is rated

Event ID
98433
Recall number
H-0546-2026
Quantity recalled
1,224,208 units

Timeline

FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.

  1. Company began the recall · Announced by the company

  2. Added to FDA's Enforcement Report · Classified by FDA

  3. In FDA's weekly enforcement report

  4. Listed on Recall Canary

  5. Recall ended

  6. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 12, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)