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Food FDA Class II Ongoing Foreign material

Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, Net Wt. 8 FL Oz (237mL) Amber PET modern round 24-400 bottle, 47 SERVING PER BOTTLE, 24 bottles- 8 FL Oz (237mL) Amber PET modern round bottles per package, Store at room. Mnfg by: Llorens Pharmaceutical Miami, FL

Llorens Pharmaceuticals International Division, Inc. Published May 27, 2026

Risk level

Class II

May cause a temporary or reversible health problem; slight chance of serious harm.

Severity score 55/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact Llorens Pharmaceuticals International Division, Inc. or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Foreign object: black particulate matter

Hazards

Black Particulate Matter · primary

Affected products (1)

Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, Net Wt. 8 FL Oz (237mL) Amber PET modern round 24-400 bottle, 47 SERVING PER BOTTLE, 24 bottles- 8 FL Oz (237mL) Amber PET modern round bottles per package, Store at room. Mnfg by: Llorens Pharmaceutical Miami, FL

4,196 units

Lot codes: B2025
Code info: Lot: B2025 Expiration Date:08/27

Affected areas

ArizonaCaliforniaColoradoDelawareFloridaGeorgiaIllinoisIndianaIowaMassachusettsMinnesotaMissouriNew JerseyNew YorkNorth CarolinaOhioOklahomaPuerto RicoTennesseeTexasVirginiaWashingtonWest VirginiaWisconsin

Timeline

  1. Initiated
    May 7, 2026
  2. Published
    May 27, 2026
Recall number
H-0809-2026
Agency
U.S. Food and Drug Administration
Country
US
Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.