Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Critical RiskFDA Food
Food & Beverages/Dietary Supplements

Wellements Iron Drops Recalled for Undeclared Milk

Agency Publication Date: August 7, 2020
Share:
Sign in to monitor this recall

Summary

Wellements LLC is recalling approximately 48,521 units of Iron Drops and Iron Drops Sampler liquid dietary supplements because they contain milk, which is not declared on the product label. People who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume these products. These supplements were distributed nationwide and sold in 1 oz (30 mL) amber glass bottles packaged in individual cartons that include an oral syringe dispenser. Consumers should return the product to the place of purchase for a refund, throw it away, or contact Wellements LLC for further instructions.

Risk

The product contains milk, an allergen not disclosed on the packaging. Consuming this product may trigger a severe or life-threatening allergic reaction in individuals with a milk allergy or sensitivity.

What You Should Do

  1. Check your supplement packaging for Iron Drops (1 oz/30 mL bottle) with UPC 729609000098 and lot numbers 18491 (Best By 1/2021) or 10592 (Best By 10/2020).
  2. Check your supplement packaging for Iron Drops Sampler (1 oz/30 mL bottle, 2 mL fill) with UPC 729609000098 and lot number 10592 (Best By 10/2020).
  3. Return the product to the place of purchase for a refund, throw it away, or contact Wellements LLC for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Wellements Iron Drops (1 oz/30 mL)
UPC Codes:
729609000098
Lot Numbers:
18491 (BB 1/2021)
10592 (BB 10/2020)

Includes a 1 mL oral syringe dispenser; Recall #: F-1147-2020

Product: Wellements Iron Drops Sampler (1 oz/30 mL, 2 mL fill)
UPC Codes:
729609000098
Lot Numbers:
10592 (BB 10/2020)

Includes a 1 mL oral syringe dispenser; Recall #: F-1148-2020

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 86110
Status: Resolved
Manufacturer: Wellements LLC
Manufactured In: United States
Units Affected: 2 products (27,557 bottles; 20,964 bottles)
Distributed To: Arizona, California, Colorado, Connecticut, Florida, Illinois, Indiana, Massachusetts, Ohio, Pennsylvania, South Carolina, Texas, Wisconsin

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. 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. Refer to the openFDA terms of service for more information.