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Class IITerminated in FDA datasetRecall initiated Mar 12, 2025

Good & Gather baby Pea, Zucchini, Kale & Thyme Vegetable Puree. Net Wt 4 oz. (113g). 6+ months.

Recalling firm: FRUSELVA USA

Why it was recalled

elevated level of lead

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 7, 2025.

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Compare the exact product and package details with the label you have.

ProductGood & 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
Package size4 oz
UPC191907993141

FDA code information

Lot Number: 4169, Best by Dec 09 2025, Lot Number: 4167, Best by Dec 07 2025.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original 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

Extracted codes and context

TypeCode / valueContext
UPC191907993141 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
best byDec 07 2025Lot Number: 4169, Best by Dec 09 2025, Lot Number: 4167, Best by Dec 07 2025.
best byDec 09 2025Lot Number: 4169, Best by Dec 09 2025, Lot Number: 4167, Best by Dec 07 2025.
lot4167Lot Number: 4169, Best by Dec 09 2025, Lot Number: 4167, Best by Dec 07 2025.
lot4169Lot Number: 4169, Best by Dec 09 2025, Lot Number: 4167, Best by Dec 07 2025.

Original FDA recall reason

elevated level of lead

Recall details

Recall number
F-0693-2025
Event ID
96501
FDA status
Terminated
Initiated
Mar 12, 2025
Reported
Apr 9, 2025
Classified
Apr 3, 2025
Terminated
May 7, 2025
Quantity
25,600 units
Location
Miami, FL, United States
Initiation type
Voluntary: Firm initiated
Notification
Other

Where it was distributed

Nationwide

FDA source record · F-0693-2025

Data updated September 16, 2026. View official FDA data ↗

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