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Use caution Food recall · FDA · Published May 7, 2026

Llorens Vitamin B-Complex Supplement Recall: Black Particulate Matter Hazard

Llorens Pharmaceuticals recalls vitamin supplements with black particles that could cause harm. Stop using affected bottles before expiration.

🇺🇸 FDA recall #H-0809-2026FoodLlorens Pharmaceuticals ›
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Recalling firmLlorens Pharmaceuticals International Division, Inc.7080 Nw 37th Ct · Miami, FL 33147-6531
✎ GovInfoNow plain-language explainer

Llorens Pharmaceuticals is recalling vitamin supplements that contain black particles. This foreign material could cause harm if ingested, so affected consumers should stop using the product. Read more at govinfonow.com/recall/6238-llorens-vitamin-b-complex-supplement-recall-black-particulate-matter-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/6238-llorens-vitamin-b-complex-supplement-recall-black-particulate-matter-hazard · Updated August 7, 2026 · Official notice: FDA #H-0809-2026

Cite this page

“Llorens Vitamin B-Complex Supplement Recall: Black Particulate Matter Hazard.” GovInfoNow, updated August 7, 2026. https://govinfonow.com/recall/6238-llorens-vitamin-b-complex-supplement-recall-black-particulate-matter-hazard. Based on FDA recall #H-0809-2026.

The FDA announced on May 7, 2026, that Llorens Pharmaceuticals International Division, Inc. voluntarily recalled Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement due to foreign object hazards. The recall affects 4,196 units distributed across multiple states.

How to tell if you have it

  • Brand: Llorens Pharmaceuticals
  • Product: Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement
  • Size: Net Wt. 8 FL Oz (237mL) Amber PET modern round 24-400 bottle
  • Lot Code: B2025
  • Expiration Date: 08/27

The hazard

The product contains black particulate matter, according to the FDA. The agency classified this as a Class II recall.

Context

GovInfoNow's records show other recent recalls of similar products include Wellnov Liposomal D3+B12 Spray Recall (2026-04-23) and Wellnov FulviLife Complex Recall (2026-04-23). A third related recall, the Wellnov Liposomal Mens 50+ Liquid Multivitamin Drops Recall, was also announced on 2026-04-23.

How to tell if you have this one

Look for bottles labeled 'Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, Net Wt. 8 FL Oz (237mL) Amber PET modern round 24-400'. The product was manufactured by Llorens Pharmaceuticals in Miami, FL with lot number B2025 and expires August 27.

  • Brand
    Llorens Pharmaceuticals
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Now

    Discard the affected bottles immediately to avoid potential harm from ingested black particles.

Where it went and when

Where it was distributed

Distributed in 23 states and Puerto Rico.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: not listedPANew Jersey: yesNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: yesCONebraska: not listedNEMissouri: yesMOKentucky: not listedKYWest Virginia: yesWVVirginia: yesVAMaryland: not listedMDDelaware: yesDEArizona: yesAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: yesFLPuerto Rico: yesPR

FDA distribution: “Distributed to MO, IL, NJ, NY, TX, FL, PR, MA, OK, VA, MN, IA, OH, GA, WI, WA, CA, IN, NC, CO, TN, MA, MO, WV, AZ, DE” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California, Colorado, Delaware, Florida, Georgia, Illinois, Indiana, Iowa, Massachusetts, Minnesota, Missouri, New Jersey, New York, North Carolina, Ohio, Oklahoma, Puerto Rico, Tennessee, Texas, Virginia, Washington, West Virginia, Wisconsin.

Recall timeline

FDA published this recall 20 days after the firm started it.

1. Firm started the recall: May 7, 202612. FDA classified it Class II: May 19, 202623. Published in FDA’s Enforcement Report: May 27, 202632026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

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

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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-0809-2026 (May 7, 2026)
  • Plain-language summary written by qwen3:4b on August 7, 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