Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement
Recalled by Llorens Pharmaceuticals International Division, Inc.
Food recall
Llorens Pharmaceuticals International Division, Inc.
Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Llorens Pharmaceuticals International Division, Inc. has recalled Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on May 27, 2026 and was initiated on May 7, 2026. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, with approximately 4,196 units affected. The company behind the recall is Llorens Pharmaceuticals International Division, Inc., based in Miami, FL. The FDA describes the product as: “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 Pharmace…”
Why was Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement recalled?
According to the FDA, the stated reason for the recall is: “Foreign object: black particulate matter.” In plain terms, this recall relates to a sterility or contamination concern.
Sterile medicines, such as injectables and eye drops, must be completely free of microorganisms and stray particles. This recall means that sterility could not be assured or that contamination was found or suspected. Using a non-sterile product of this kind can cause infections, which is why these recalls are treated seriously.
What should you do?
If you think you may have bought Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement, compare it against the product description and identifying codes (Lot: B2025 Expiration Date:08/27) before using it. This recall is currently listed as ongoing.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Llorens Pharmaceuticals International Division, Inc. or your local health authority.
About this recall
This recall was distributed in FL. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Who this recall affects
This recall matters to anyone who bought Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement. Even if you feel fine, it's worth checking what you have on hand rather than assuming you were missed.
Distribution listed in the notice: 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.
What sterility or contamination concern actually means
Sterile medicines, such as injectables and eye drops, must be completely free of microorganisms and stray particles. This recall means that sterility could not be assured or that contamination was found or suspected. Using a non-sterile product of this kind can cause infections, which is why these recalls are treated seriously.
In this case, the concern applies specifically to Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement from Llorens Pharmaceuticals International Division, Inc. — not to the wider category of products. Similar items from other brands aren't part of this recall.
How to check whether you have it
On packaged food, lot codes and best-by dates are usually printed in small date-coding ink on the side seam, the bottom of the package, or near the top seal — not on the front label. The UPC barcode is on the back or bottom.
Compare what you find against the identifying details in this recall: Lot: B2025 Expiration Date:08/27
What to do if you already bought it
Do not eat the product, even if it looks and smells normal — contamination is usually invisible.
Return it to the store for a refund, or throw it away in a sealed bag so pets and wildlife can't reach it.
If it touched other food or surfaces, wash those surfaces and your hands with hot soapy water. When in doubt, contact Llorens Pharmaceuticals International Division, Inc. or your local health department.
Full recall details
- Status
- Ongoing
- Date reported
- May 27, 2026
- Recall started
- May 7, 2026
- Distributed in
- FL
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement recalled?+
According to the FDA: Foreign object: black particulate matter
How serious is this recall?+
Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
What should I do if I have Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0809-2026. Information last synced from the FDA on August 20, 2026.