Food Recall Check
Class II · Moderate risk Terminated Initiated Jan 21, 2019 (8 years ago)

Parent's Choice Toddler Next Stage¿ Milk Drink Powder Natural… recall

Recalled by PBM Nutritionals, LLC · Milton, VT, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Product may contain foreign material.

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

Parent's Choice Toddler Next Stage¿ Milk Drink Powder Natural Milk Flavor With Other Natural Flavors, Stage 3, 1 Year and Up, NET WT 24 OZ (1.5 LB) 680g, UPC: 0 78742 06717 9 and Little JOURNEY Toddler Next Stage MILK DRINK POWDER, NET WT I PESO NETO 24 OZ I ONZAS (1.5 LB) 680g.

Quantity: 18,632 cans

Food: Milk & dairy Baby food & infant formula

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 Codes: T16DTKC, T17DTJC, T20DTDC

Where it was sold

Alabama Arkansas Arizona California Colorado Connecticut Delaware Florida Georgia Iowa Illinois Indiana Kansas Kentucky Louisiana Michigan Minnesota Missouri Mississippi North Carolina New Hampshire New York Ohio Oregon Pennsylvania Tennessee Texas Utah Virginia Wisconsin

FDA's distribution note: AL AR AZ CA CO CT DE FL GA IA IL IN KS KY LA MI MN MO MS NC NH NY OH OR PA TN TX UT VA WI

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
PBM Nutritionals, LLC
Initiated by
FDA Mandated
Recall initiated
Jan 21, 2019
In FDA report of
Feb 20, 2019
Terminated
May 29, 2019
FDA recall number
F-0904-2019 · event 81985
Official record
FDA enforcement report search

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