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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Food
Food & Beverages/Dietary Supplements

Rosabella Moringa Capsules Recalled for Possible Salmonella Contamination

Agency Publication Date: March 9, 2026
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Summary

Ambrosia Brands LLC is recalling approximately 1,224,208 bottles of Rosabella brand Moringa dietary supplement capsules due to potential contamination with Salmonella. The recall affects 60-count bottles distributed nationwide in the United States and several international territories. Consumers should immediately stop using these supplements and return them to the place of purchase for a full refund.

Risk

The product may be contaminated with Salmonella, an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy individuals may experience fever, diarrhea, nausea, vomiting, and abdominal pain.

What You Should Do

  1. Check your bottle of Rosabella MORINGA dietary supplement (60 capsules) for UPC 8 60012 16172 0.
  2. Check the lot number and expiration date printed on your bottle against the list of 52 affected codes, which includes lots such as 5020591 through 5020596 (Exp 03/2027) and 5100048 (Exp 11/2027). See the Affected Products section below for the full list of affected codes.
  3. Return the product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

💰Option 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
🗑️Option 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Rosabella MORINGA dietary supplement capsules (60 capsules)
UPC Codes:
860012161720
Lot Numbers (52):
5020591 (03/2027)
5020592 (03/2027)
5020593 (03/2027)
5020594 (03/2027)
5020595 (03/2027)
5020596 (03/2027)
5030246 (04/2027)
5030247 (04/2027)
5030248 (04/2027)
5030249 (04/2027)
5030250 (04/2027)
5030251 (04/2027)
5040270 (05/2027)
5040271 (05/2027)
5040272 (05/2027)
5040273 (05/2027)
5040274 (05/2027)
5040275 (05/2027)
5040276 (05/2027)
5040277 (05/2027)
5040278 (05/2027)
5040279 (05/2027)
5050053 (6/2027)
5050054 (6/2027)
5050055 (6/2027)
5050056 (6/2027)
5060069 (07/2027)
5060070 (07/2027)
5060071 (07/2027)
5060072 (07/2027)
5060073 (07/2027)
5060074 (07/2027)
5060075 (07/2027)
5060076 (07/2027)
5060077 (07/2027)
5060078 (07/2027)
5060079 (07/2027)
5060080 (07/2027)
5080084 (9/2027)
5080085 (9/2027)
5080086 (9/2027)
5090107 (10/2027)
5090108 (10/2027)
5090109 (10/2027)
5090113 (10/2027)
5090114 (10/2027)
5090115 (10/2027)
5090116 (10/2027)
5090117 (10/2027)
5090118 (10/2027)

Distributed by Ambrosia Brands, LLC, 625 Randall Ave, St. 100, Cheyenne, WY 82001.

Product Images

Photograph of Rosabella Moringa, 60 capsules bottle

Photograph of Rosabella Moringa, 60 capsules bottle

Photograph of product code placement for Rosabella Moringa, 60 capsules bottle

Photograph of product code placement for Rosabella Moringa, 60 capsules bottle

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98433
Status: Active
Manufacturer: Ambrosia Brands LLC
Sold By: retailers nationwide; international distributors
Manufactured In: United States
Units Affected: 1,224,208 units
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · FDA Press Release · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.