Skip to main content
High RiskFDAfda-H-0005-2025CHEMICAL EXPOSURE

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 pouc...

Category
Units Affected
53,620
Recall Date
May 9, 2025
Issuing Agency
Hazard
Chemical Exposure

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-H-0005-2025.

Elevated levels of Lead, cadmium and arsenic

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-H-0005-2025.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Publix Super Markets, Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-H-0005-2025.

Publix Super Markets, Inc.

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

Visit FDA.gov →

📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

How to report to FDAFile a report at FDA

Publix Super Markets, Inc. Recall FAQ

Publix Super Markets, Inc. is the subject of a produce safety report: 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 pouc.... The notice was published on May 9, 2025 by the U.S. Food and Drug Administration (FDA). Approximately 53,620 units are potentially affected.