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
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 2025 | Recall initiated by company | |
| 3 Apr 2025 | Classified by FDA | +22 days |
| 9 Apr 2025 | Published 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
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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