Food Recall Check
Class I · High risk Terminated Initiated Jul 23, 2020 (6 years ago)

UpSpring Baby Iron + Immunity MULTI + IRON + ZINC Promotes… recall

Recalled by Upspring,ltd · Austin, TX, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

May contain undeclared milk

Undeclared allergen: Milk

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

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 No: 859188006805 packaged in dark brown glass bottles and placed in paper carton with dropper supplier in carton

Quantity: 10,328 units

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

lot # 06691

Where it was sold

Nationwide.

FDA's distribution note: Nationwide throughout the US and China, Singapore, Vietnam, Hong Kong .

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Upspring,ltd
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 23, 2020
In FDA report of
Aug 19, 2020
Terminated
Jun 3, 2021
FDA recall number
F-1149-2020 · event 86103
Official record
FDA enforcement report search