Class IIOngoingVoluntary: Firm initiated
Llorens Pharmaceuticals International Division, Inc.: food recall H-0809-2026
Llorens Pharmaceuticals International Division, Inc. of Miami, FL recalled Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, Net Wt. 8 FL Oz (237mL) Amber PET modern round 24-400… Reason: Foreign object: black particulate matter. The FDA listed it as Class II in its Enforcement Report dated May 27, 2026; distribution: Arizona, California, Colorado, Delaware, Florida, Georgia, Iowa, Illinois, Indiana, Massachusetts, Minnesota, Missouri, North Carolina, New Jersey, New York, Ohio, Oklahoma, Puerto Rico, Tennessee, Texas, Virginia, Washington, Wisconsin, West Virginia.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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
- Product quantity
- 4,196 units
- Reason for recall
- Foreign object: black particulate matter
- Codes, lots and dates on the package
- Lot: B2025 Expiration Date:08/27
- Distribution pattern
- 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
- Recalling firm
- Llorens Pharmaceuticals International Division, Inc., Miami, FL
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Letter
Advertisement
Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | May 7, 2026 |
| Classified by the FDA | May 19, 2026 |
| Published in the Enforcement Report | May 27, 2026 |
Advertisement
OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0809-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- 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. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.