FDA Enforcement Weekly: Supplements, Cosmetics & Food The FDA actions that actually touch your world, in plain English. For QA & regulatory teams.

This summer's batch: 7 Class I Salmonella recalls of moringa and greens powders, including one bulk supplier · 2 CGMP warning letters to cosmetics contract manufacturers · a wave of 15+ FSVP warning letters to small importers · an undeclared-egg trio (two in "vegan" products).

⭐ Item of the week: seven Class I recalls, eleven weeks, one ingredient

Between May 22 and August 7, six firms ran seven separate Class I Salmonella recalls of moringa and greens powder products. All verified in openFDA, recall numbers inline:

• 🔴 Total Nutrition Inc. (TNVitamins / Doctor's Pride, Farmingdale NY), twice: Green Superfood Moringa capsules May 22 (H-0942-2026), then 100% Organic Moringa capsules and powder June 26 (H-1185-2026). Also a repeat from FDA's 2018 warning letter.
• 🔴 MOGO Moringa LLC (St. Louis, MO), pure moringa capsules sold on Amazon, eBay and Etsy, May 24 (H-1128-2026).
• 🔴 Trafa Pharmaceutical Inc. (Chicopee, MA), organic moringa leaf powder, June 24 (H-1144-2026).
• 🔴 Green Jeeva LLC (Cerritos, CA), the one to stare at: bulk 15 kg bags of moringa powder, an ingredient, recalled July 8 after testing positive, already shipped to four downstream manufacturers "for further processing and distribution" (H-1180-2026).
• 🔴 Zen Principle Naturals moringa capsules (brand: Relay Peak Research LLC; the enforcement record sits under manufacturer Factory6, Inc., Lindon UT), July 19, after FDA testing of the incoming moringa powder came back positive. Sold nationwide via Amazon since December (FDA announcement, H-1222-2026).
• 🔴 Lexunder Inc. (Food To Live, Brooklyn NY), moringa, supergreens, kale, wheatgrass, spirulina and algae powders, August 7, after an FDA retail sample tested positive (FDA announcement; enforcement number pending). Also a repeat: the same brand's moringa and supergreens were recalled in November 2025 (H-0309/H-0310-2026).

Why it happened (plain English): powdered botanicals are dried agricultural products: leaves, grasses, roots. Drying doesn't kill Salmonella; it preserves it. It survives in low-moisture powders for years, and encapsulation adds no kill step. The Green Jeeva recall shows the mechanism in one line: one bulk lot tests positive, and four manufacturers who bought it on the strength of paperwork now own the problem.

Who else should care: anyone selling powdered botanicals: capsules, blends, smoothie mixes, gummies with botanical inputs. Your supplier's COA is not a kill step. If your micro-verification of incoming botanical powder is "the certificate said it was clean," you are running the same process these firms were running in May. Two of the six are repeat visitors; the pattern does not fix itself.

Verify: every recall number above is searchable in FDA's enforcement database.

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Also this summer

• 🟡 Two cosmetics contract manufacturers drew CGMP warning letters. Woodbine Products Company (Medina, OH), cited July 27 for no identity testing of incoming ingredients, including the tests that catch diethylene glycol (DEG) substitution, the contaminant behind historic mass poisonings, plus no process validation and a weak quality unit (FDA letter). CoValence Laboratories (Chandler, AZ), a skincare/OTC contract manufacturer, cited July 16 for CGMP violations (FDA letter). Why it matters: if either firm makes your product, these letters are about your product, and your brand name appears nowhere in them. That's the co-manufacturer problem in one sentence: their letter, your shelf.

• ⚪ The undeclared-egg trio. 529 Commerce's "Rooted in Rare" aquafaba powder, a vegan egg replacer, recalled for undeclared egg (FDA announcement). Blank Slate Creamery's vegan frozen dessert sandwiches: also undeclared egg. Jaime's Foods ATX jalapeño ranch dressing: undeclared egg, August 26. Why it matters: two of the three sold products marketed as egg-free. A "free-from" claim doesn't change your allergen-control obligations. It raises the cost of the same failure, because your buyer chose you specifically to avoid the allergen.

📈 Watching for patterns

Fifteen-plus warning letters to small food importers this summer, all for the same thing: no Foreign Supplier Verification Program at all. Produce, canned goods, dairy, sauces, tea, pet treats: the products vary, the citation doesn't. Reading the letters, many of these firms clearly didn't know the rule applied to them. If you import any ingredient or finished food, even as a side line, you are an "importer" under FSMA, and FDA spent the summer proving it checks.

✅ If you do one thing this week

If you sell powdered botanicals: pull your last verification test on incoming powder (your own micro result, not the supplier's COA) and check the date. If you use a contract manufacturer (cosmetics or supplements): search FDA's warning letter database for their name, today. Then decide how you'd find out next time without luck. If you import anything: confirm a written FSVP exists for every supplier/ingredient pair you bring in.

Question for you this week: when a supplier or contract manufacturer of yours has a problem, how do you find out today: them telling you, the news, or luck? Hit reply, we read every answer.

And if you'd want alerts the moment one of YOUR suppliers, co-manufacturers, or competitors is cited, instead of checking FDA yourself, reply "watchlist" for early access.

FDA Enforcement Weekly is built from public FDA data by a small team that reads every enforcement action so you don't have to. Not affiliated with the FDA. Unsubscribe · Forward to a colleague who'd want this.