CLASS II Food recall · Reported 9 Apr 2025 · FDA Enforcement Report

Good & Gather baby Pea, Zucchini, Kale & Thyme Vegetable Puree recalled

Fruselva U is recalling Good & Gather baby Pea, Zucchini, Kale & Thyme Vegetable Puree, distributed nationwide in the US. The recall was initiated on 12 Mar 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Number: 4169, Best by Dec 09 2025, Lot Number: 4167, Best by Dec 07 2025.
Quantity recalled25,600 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0693-2025
FDA event ID
96501
Recalling firm
Fruselva U, Miami, FL
Brand
Good
Classification
Class II
Status
Terminated
Recall initiated
12 Mar 2025
FDA classified
3 Apr 2025
Reported
9 Apr 2025
Type
Voluntary: Firm initiated
Customers notified by
Other
Reason category
Lead & Heavy Metals
Product category
Lettuce

Timeline

12 Mar 2025Recall initiated by company
3 Apr 2025Classified by FDA+22 days
9 Apr 2025Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

elevated level of lead

Lead and other heavy metals accumulate in the body. Children are most at risk; even low levels can affect development.

Product as listed by the FDA

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

Where it was distributed

Nationwide

Nationwide

Stores named: Target

Questions about this recall

Why was it recalled?

elevated level of lead

Which lots are affected?

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

Where was it sold?

Nationwide

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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