FDA recall, , Moderate risk
Nephronex Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral Liquid
The oral liquid supplement contains black particles in the liquid.
Summary by Recall Canary from the FDA notice
What happened
Safecor Health, LLC of Columbus, Ohio recalled Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral Liquid, Contains: Folic Acid 799 mcg/5mL, Delivers 5 mL per oral syringe, (Nephronex), Mfg By: LLORENS; Pkg by: Safecor, Columbus, OH, because black particles were observed in the liquid. The recall began May 1, 2026, and was added to the FDA's Enforcement Report on May 21, 2026, with 520 syringes affected.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is yours affected?
Affected if its NDC or UPC is listed.
A UPC is the number printed under a barcode. An NDC (National Drug Code) is usually printed on the drug's label.
Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral Liquid
- NDC
- 54859-0516-08
- UPC
- 26110722
- 26110743
- 26111218
Recall details
- Company began the recall
- Sold in
- Company
- Safecor Health, LLCColumbus, Ohio
- Hazard
- Foreign object
- Risk
Moderate risk
Taking it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98899
- Recall number
- D-0549-2026
- Quantity recalled
- 520 syringes
All recalls from Safecor Health, LLC
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
