Severity
Critical
CriticalClass IOngoing
FDA Food recall · Reported July 8, 2026
MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, 180 QUICK RELEASE VEGGIE CAPSULE, 100% PURE, 350 MG PER CAPSULE, SUPPLEMENT FACTS MORINGA POWDER 1050 mg, Ingredients: 100% Pure Moringa Leaf Powder (Moringa Oleifera), MANUFACTURED IN USA AND Marketed by: MOGO MIRINGA LLC, PO BOX 32066 Saint Louis, MO 63132
Product may be contaminated with Salmonella Typhimurium
Mogo Moringa LLC recalled MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, 180 QUICK RELEASE VEGGIE CAPSULE,… - a critical-severity action.
MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, 180 QUICK RELEASE VEGGIE CAPSULE,… was recalled by Mogo Moringa LLC in July 8, 2026. Reason: Product may be contaminated with Salmonella Typhimurium. Check the official notice for the remedy. Verify recall #H-1128-2026 with the FDA Food before acting.
The recall
Mogo Moringa LLC issued this critical-severity FDA Food recall-Product may be contaminated with Salmonella Typhimurium.
- Critical
- severity level
- Class I
- classification
- July 8, 2026
- reported
Sourced from official FDA Food enforcement records. Verify recall #H-1128-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #H-1128-2026) was formally reported on July 8, 2026, with the manufacturer initiating the action on May 24, 2026. It is classified under Critical severity (Class I), with a current status of Ongoing. Mogo Moringa LLC is listed as the recalling firm, operating out of Saint Louis, MO. Federal records list the affected scope as 23,186 bottles.
The documented reason for this recall is: Product may be contaminated with Salmonella Typhimurium Distribution data in the federal record shows the product reached: Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com). Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,436 drugs & medications recalls on record
Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
23,186 bottles
Related Recalls
6
0 from same agency
Product description
MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, 180 QUICK RELEASE VEGGIE CAPSULE, 100% PURE, 350 MG PER CAPSULE, SUPPLEMENT FACTS MORINGA POWDER 1050 mg, Ingredients: 100% Pure Moringa Leaf Powder (Moringa Oleifera), MANUFACTURED IN USA AND Marketed by: MOGO MIRINGA LLC, PO BOX 32066 Saint Louis, MO 63132
Reason for recall
Product may be contaminated with Salmonella Typhimurium
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Ongoing |
| Recall number | H-1128-2026 |
| Date reported | July 8, 2026 |
| Date initiated | May 24, 2026 |
| Recalling firm | Mogo Moringa LLC |
| Firm location | Saint Louis, MO |
| Affected scope | 23,186 bottles |
| Distribution | Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com) |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (H-1128-2026) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, 180 QUICK RELEASE VEGGIE CAPSULE, 100% PURE, 350 MG PER CAPSULE, SUPPLEMENT FACTS MORINGA POWDER 1050 mg, Ingredients: 100% Pure Moringa Leaf Powder (Moringa Oleifera), MANUFACTURED IN USA AND Marketed by: MOGO MIRINGA LLC, PO BOX 32066 Saint Louis, MO 63132. Recalled by Mogo Moringa LLC. Units affected: 23,186 bottles.
Why was this product recalled? ▼
Product may be contaminated with Salmonella Typhimurium
Which agency issued this recall? ▼
This recall was issued by the FDA Food on July 8, 2026. Severity: Critical. Recall number: H-1128-2026.
Where was the recalled product distributed? ▼
Distribution: Products were sold nationwide via ecommerce (Amazon, Ebay, Etsy, and mogomiranga.com).
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (H-1128-2026) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nationwide recalls with similar severity or category timing
Two federal-filing-derived peer sets for this notice, both outside the same recalling firm and filing state so the neighborhoods are not firm or geographic containment.
Similar severity · nearest report date
Same archive severity grade (Critical), closest by report date among other firms and states.
Similar Drugs & Medications · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
Showing 5 of 14436 other recalls in this category.
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Rohto-Mentholatum (Vietnam) Co., Ltd. · 2026-07-29
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Major Pharmaceuticals · 2026-07-29
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported July 8, 2026. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.