RecallHawk
Class II Recall

Greenwise Pear Kiwi Spinach & Pea Baby Food Pouch. Net Wt 4 oz. (113g). Stage 2 6 months+, Best if" date of 11/01/2025.

Publix Super Markets, Inc.

Summary

The FDA issued a Class II for Greenwise Pear Kiwi Spinach & Pea Baby Food Pouch. Net Wt 4 oz. (113g). Stage 2 by Publix Super Markets, Inc.. Reason: Elevated levels of Lead, cadmium and arsenic.

Details

Source

Food Recall

External ID

H-0005-2025

Action Date

2025-06-11

Status

Terminated

Category

food

Product Description

Greenwise Pear Kiwi Spinach & Pea Baby Food Pouch. Net Wt 4 oz. (113g). Stage 2 6 months+, Best if" date of 11/01/2025. Packed in 14 pouches per case, 4 oz per pouch. Distributed by Publix Super Markets, Inc. 3300 Publix Corporate Parkway Lakeland, FL 33881.

Lot/Code Info: Lot Code 24BA306 best-used-by date of 11-01-2025 Global Trade Item Number is 41414-00901

Quantity Affected: 53620 units equaling 3830 cases

Reason for Recall

Elevated levels of Lead, cadmium and arsenic

Distribution

FL, GA, SC, NC, TN, AL, VA, KY

Type: Voluntary: Firm initiated

Recall Initiated: 2025-05-09

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 123 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Publix Super Markets, Inc. has 10 FDA actions in our database, including 10 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Publix Super Markets, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Publix Super Markets, Inc. have FDA actions?

Publix Super Markets, Inc. has 10 FDA actions in our database, including 10 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0005-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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