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Lower risk Food recall · FDA · Published July 23, 2020

Upspring Baby Iron Supplement May Contain Undeclared Milk - Recall

Upspring recalls baby iron supplements that may contain undeclared milk. This poses a risk for infants with milk allergies. Consumers should check product labels and contact Upspring for details.

🇺🇸 FDA recall #F-1149-2020FoodUpspring ›
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Recalling firmUpspring,ltd4209 S Industrial Dr Ste 200 · Austin, TX 78744-1053
✎ GovInfoNow plain-language explainer

Upspring has recalled baby iron supplements that may contain undeclared milk, which could cause allergic reactions in infants. This is a safety issue for babies with milk allergies. Read more at govinfonow.com/recall/15475-upspring-baby-iron-supplement-may-contain-undeclared-milk-recall.

Source Summary by GovInfoNow · govinfonow.com/recall/15475-upspring-baby-iron-supplement-may-contain-undeclared-milk-recall · Updated October 5, 2026 · FDA enforcement record: FDA #F-1149-2020

Cite this page

“Upspring Baby Iron Supplement May Contain Undeclared Milk - Recall.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/15475-upspring-baby-iron-supplement-may-contain-undeclared-milk-recall. Based on FDA recall #F-1149-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1149-2020%22&limit=1).

Upspring,ltd recalled UpSpring Baby Iron + Immunity MULTI + IRON + ZINC dietary supplements due to undeclared milk allergens, the FDA announced on July 23, 2020. Consumers should stop using the product and contact the company for a refund.

How to tell if you have it

  • Brand: Upspring
  • Product: UpSpring Baby Iron + Immunity MULTI + IRON + ZINC Promotes nutrition For Healthy Growth + Immune System Support For Infants 4 months + Natural Grape Flavor Easy To Use Dropper Dietary Supplement NET WT 2 FL OZ (60 ML)
  • UPC: 859188006805
  • Lot code: 06691
  • Units affected: 10,328

The hazard

The product may contain undeclared milk, posing an allergy risk to consumers. The FDA issued this recall notice on July 23, 2020.

Context

GovInfoNow's records show other recent recalls of similar products include Imu-Tek Immuno-5 Colostrum Powder Recall (2025-11-25) and Fayus OLA-OLA Pounded Yam Recall (2026-07-06). Baby Allergy Herbal Supplement Recall occurred on 2025-11-20.

How to tell if you have this one

The product is labeled 'UpSpring Baby Iron + Immunity MULTI + IRON + ZINC' and comes in dark brown glass bottles with a dropper. It was sold with lot number 06691.

  • Brand
    Upspring
  • Product
    UpSpring Baby Iron + Immunity MULTI + IRON + ZINC Promotes nutrition For Healthy Growth + Immune System Support For
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the product name and lot number on the label to confirm if it's recalled.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide throughout the US and China, Singapore, Vietnam, Hong Kong .” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 10 months after the firm started it.

1. Firm started the recall: Jul 23, 202012. FDA classified it Class I: Aug 7, 202023. Published in FDA’s Enforcement Report: Aug 19, 202034. FDA terminated the recall: Jun 3, 2021420202021
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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-1149-2020 (July 23, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1149-2020 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA