Lower riskFood recall · FDA · Published July 24, 2020
Wellements Iron Drops Dietary Supplement Recall: Undeclared Milk Hazard
Wellements LLC recalls Iron Drops liquid dietary supplements due to undeclared milk content. Consumers should check product labels for UPC 729609000098 and lots 18491 BB (1/2021) or 10592 BB (10/2020).
“Wellements Iron Drops Dietary Supplement Recall: Undeclared Milk Hazard.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/15468-wellements-iron-drops-dietary-supplement-recall-undeclared-milk-hazard. Based on FDA recall #F-1147-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1147-2020%22&limit=1).
The FDA announced on July 24, 2020, that Wellements LLC voluntarily recalled Iron Drops liquid dietary supplement due to undeclared milk. The recall affects approximately 27,557 bottles distributed nationwide.
How to tell if you have it
Brand: Wellements
Product: Iron Drops (UPC 729609000098) liquid Dietary Supplement, 1 oz/30 mL amber glass bottle packaged in an individual product carton that includes a 1 mL oral syringe dispenser.
Lot codes: 18491 BB 1/2021, Lot 10592 BB 10/2020
The hazard
The product contains undeclared milk, posing a risk to consumers with milk allergies or sensitivities. The FDA classified this as a Class I recall.
Context
GovInfoNow's records show the brand has been involved in other recent recalls of similar products include Fayus OLA-OLA Pounded Yam Recall (2026-07-06) and Winfield's CWB Chocolate Bar Recall (2026-04-27). Other recent recalls of similar products include Vital Nutrients Aller-C Recall (2026-03-27).
How to tell if you have this one
Check for the UPC 729609000098 on the product label. Look for lot numbers 18491 BB (1/2021) or 10592 BB (10/2020) on the packaging.
Brand
Wellements
Product
Iron Drops (UPC 729609000098) liquid Dietary Supplement, 1 oz/30 mL amber glass bottle packaged in an individual
Category
Food
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class I
Status
Terminated
Distribution
Nationwide. AZ, CA, CO, CT, FL, IL, IN, MA, OH, PA, SC, TX, WI.
Recall number
Product, codes & lots
Quantity
F-1147-2020
Iron Drops (UPC 729609000098) liquid Dietary Supplement, 1 oz/30 mL amber glass bottle packaged in an individual product carton that includes a 1 mL oral syringe dispenser.; Lot 18491 BB 1/2021, Lot 10592 BB 10/2020
27,557 bottles
F-1148-2020
Iron Drops Sampler (UPC 729609000098) liquid Dietary Supplement, 1 oz/30 mL, (2 mL fill) amber glass bottle packaged in an individual product carton that includes a 1 mL oral syringe dispenser.; Lot 10592 BB 10/2020
20,964 bottles
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the UPC 729609000098 and lot numbers 18491 BB (1/2021) or 10592 BB (10/2020) on the product.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 13 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Nationwide. AZ, CA, CO, CT, FL, IL, IN, MA, OH, PA, SC, TX, WI.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Arizona, California, Colorado, Connecticut, Florida, Illinois, Indiana, Massachusetts, Ohio, Pennsylvania, South Carolina, Texas, Wisconsin.
Recall timeline
FDA terminated this recall 6 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-1147-2020 (July 24, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1147-2020 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.