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FDA recall record

H-E-B GROCERY HEB Baby Sweet Potato Recall

This page is a permanent record of a food recall announced by the U.S. Food and Drug Administration (FDA). It is kept online for reference; it does not mean this product is being recalled today or is currently on store shelves. Details are reproduced from the FDA enforcement report.
SourceFDA
FDA recall numberF-0713-2017
Recall initiatedNovember 18, 2016
Recall classClass II
FDA statusTerminated
Recalling firmH-E-B GROCERY COMPANY LP DBA HEB
ProductHEB Baby Sweet Potato 4 ounce cups, 2 pack packaged in plastic cups with a cardboard sleeve

Why it was recalled

The reason below is reproduced from the official FDA enforcement report.

Customer reported a small piece of rubber inside one variety of the recalled product.

Is your package affected?

The FDA enforcement report lists the following identifiers for this recall. Match them against the codes printed on your package.

UPC codes named in the recall

The FDA enforcement report for this recall does not list UPC codes.

Lot / batch codes named in the recall

Product description from the FDA enforcement report:

HEB Baby Sweet Potato 4 ounce cups, 2 pack packaged in plastic cups with a cardboard sleeve

A recall almost never means "every jar of this brand, ever." It means a specific run of a specific product. To know whether the package in your kitchen is affected, you need to match the identifiers in the recall notice against the ones printed on your package:

If the notice lists specific lot codes and yours isn't on the list, your package likely isn't part of the recall. If you can't find the codes, or they're worn off, the safe move is to treat it as recalled and not feed it.

If your product is recalled: stop using it. Most notices tell you to either dispose of it or return it to the store for a refund. Don't donate it or pass it along. If your child has already eaten it and you have any concern, call your pediatrician, and in an emergency call 911 (US) or your local emergency number.

Recall classes: how serious is it?

The FDA sorts recalls into three classes by how much risk the product poses. Knowing the class tells you how urgently to act.

Class What it means Plain-English read
Class I "A reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death." The most serious. Stop using it now. Undeclared allergens are the leading cause of Class I food recalls, and serious contamination recalls land here too.
Class II Use "may cause temporary or medically reversible adverse health consequences," or the risk of serious harm is remote. Real but lower risk. Still worth acting on.
Class III Use is "not likely to cause adverse health consequences." Usually a labeling or quality issue, not a safety emergency.

Official FDA notice

This recall is published in the FDA enforcement report database under recall number F-0713-2017. Source: FDA.

View the official FDA enforcement record (opens the openFDA data record for this recall).

Search current FDA recalls, market withdrawals, and safety alerts on the FDA website.

Check future recalls automatically

The AllerSee scanner built into Baby Ledger AI cross-checks every barcode you scan against the FDA recall feed automatically, and cross-references the ingredients against your own child's allergen profile at the same time. The allergen and recall checks are free and unlimited on every plan. It's there so you don't have to refresh a government website every morning, not as a substitute for the official sources or for your pediatrician's guidance.

All baby & infant food recalls · Guide: How to Check If Your Baby's Food Has Been Recalled

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This article is general information to help you stay aware of food recalls and labels. It is not medical advice and not a substitute for professional guidance. Baby Ledger AI and AllerSee are informational, label-reading tools, not medical devices, and they do not diagnose, treat, prevent, or protect against any allergy or medical condition. Our recall cross-check runs against the FDA recall feed and does not cover every recall. Always read the full product label, check the official government recall sources, and consult your pediatrician or a qualified medical professional for any allergy or health concern. In a suspected allergic reaction or medical emergency, call 911 (US) or your local emergency number. AllerSee™ is a trademark of Fong Shui Labs LLC. AllerSee's allergen detection approach is patent-pending.

Baby Ledger AI is not affiliated with, endorsed by, or certified by the U.S. Food and Drug Administration. Recall information is reproduced from publicly available FDA records.