Food, drugs, devices › Publix Super Markets, Inc.
Food 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.
FDA enforcement event 96883 is a food recall by Publix Super Markets, Inc. of Lakeland, FL, initiated 9 May 2025 and classified Class II, with 1 product record.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 54% of the 569 food enforcement events initiated in 2025 carry the same class.
Status: Terminated, terminated 16 Jun 2025. Initiation: voluntary: firm initiated. Publix Super Markets, Inc. has 18 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Publix Super Markets, Inc., Lakeland, FL.
Reason for recall
"Elevated levels of Lead, cadmium and arsenic"
Distribution
"FL, GA, SC, NC, TN, AL, VA, KY"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| H-0005-2025 | 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. | 53620 units equaling 3830 cases | Class II | Terminated | 11 Jun 2025 |
Context
Other enforcement events for Publix Super Markets, Inc.
All 18 events for Publix Super Markets, Inc.
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Elevated levels of Lead, cadmium and arsenic"
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "FL, GA, SC, NC, TN, AL, VA, KY"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 16 Jun 2025. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.