Good & Gather baby Pea, Zucchini, Kale & Thyme Vegetable Puree. Net Wt 4 oz. (113g). 6+ months. UPC 1 91907-99314 1.
Summary
The FDA issued a Class II for Good & Gather baby Pea, Zucchini, Kale & Thyme Vegetable Puree. Net Wt 4 oz. (1 by FRUSELVA USA. Reason: elevated level of lead.
Details
Source
Food Recall
External ID
F-0693-2025
Action Date
2025-04-09
Status
Terminated
Category
food
Product Description
Good & Gather baby Pea, Zucchini, Kale & Thyme Vegetable Puree. Net Wt 4 oz. (113g). 6+ months. UPC 1 91907-99314 1. Distributed by Target Corporation, Minneapolis, MN 55403. Product of Colombia
Lot/Code Info: Lot Number: 4169, Best by Dec 09 2025, Lot Number: 4167, Best by Dec 07 2025.
Quantity Affected: 25,600 units
Reason for Recall
elevated level of lead
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2025-03-12
Company
Miami, FL
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 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (FRUSELVA USA) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does FRUSELVA USA have FDA actions?
This is the only FDA action we have on record for FRUSELVA USA in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0693-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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