GERBER Organic 2ND FOODS Pears, Carrots & Peas, 3.5 oz., film pouches, 6 pouches per display box/ 2 display boxes per case; Asst Ecom PK...
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1093-2016.
Gerber is voluntarily recalling two batches of GERBER¿ Organic 2ND FOODS¿ Pouches, varieties Pears, Carrots & Peas; and Carrots, Apples & Mangoes because the products produced do not meet quality standards. The packaging may contain air holes, which could result in product spoilage from mold and yeast growth, as well as an off smell and taste.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1093-2016.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Nestle Infant Nutrition or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- 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-F-1093-2016.
Nestle Infant Nutrition
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.
Nestle Infant Nutrition Recall FAQ
Nestle Infant Nutrition is the subject of a food safety report: GERBER Organic 2ND FOODS Pears, Carrots & Peas, 3.5 oz., film pouches, 6 pouches per display box/ 2 display boxes per case; Asst Ecom PK.... The notice was published on March 24, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 51,945,335 units are potentially affected.