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Use caution Food recall · FDA · Published March 24, 2016

Gerber Organic Baby Food Recall: Spoilage Risk in Pears, Carrots & Peas

Gerber is recalling specific batches of Organic 2nd Foods pouches due to packaging defects that may cause spoilage from mold and yeast growth.

🇺🇸 FDA recall #F-1093-2016FoodGerber ›
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Recalling firmNestle Infant Nutrition12 Vreeland Rd Fl 2, PO Box 697 · Florham Park, NJ 07932-0697
✎ GovInfoNow plain-language explainer

What happened, in plain English

Nestle Infant Nutrition is voluntarily recalling two batches of Gerber Organic 2nd Foods pouches, specifically the Pears, Carrots & Peas variety. The issue stems from packaging defects that create air holes, potentially leading to product spoilage via mold and yeast growth. Consumers should check their products against the specific batch numbers and expiration dates listed in the recall notice. Read more at govinfonow.com/recall/24962-gerber-organic-baby-food-recall-spoilage-risk-in-pears-carrots.

Source Summary by GovInfoNow · govinfonow.com/recall/24962-gerber-organic-baby-food-recall-spoilage-risk-in-pears-carrots · Updated October 11, 2026 · FDA enforcement record: FDA #F-1093-2016

Cite this page

“Gerber Organic Baby Food Recall: Spoilage Risk in Pears, Carrots & Peas.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/24962-gerber-organic-baby-food-recall-spoilage-risk-in-pears-carrots. Based on FDA recall #F-1093-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1093-2016%22&limit=1).

Why it’s dangerous

The packaging may contain air holes that allow mold and yeast to grow inside the pouch. This spoilage can result in an off smell and taste, posing a health risk if consumed.

Who’s affected

Parents or caregivers who purchased Gerber Organic 2nd Foods Pears, Carrots & Peas pouches between July 2015 and March 2016. Infants consuming these specific batches are at risk if the product has spoiled.

How to tell if you have this one

Look for Gerber Organic 2nd Foods Pears, Carrots & Peas, 3.5 oz. film pouches. Check the bottom of the pouch for Batch numbers starting with 51945335XX (Best By July 12, 2016) or 51955335XX (Best By July 13, 2016). The product was sold in domestic states including AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, NC, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, VA, WA, WI.

  • Brand
    Gerber
  • Product
    GERBER Organic 2ND FOODS Pears, Carrots & Peas, 3.5 oz., film pouches, 6 pouches per display box/ 2 display boxes per
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Domestic: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, NC, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, VA, WA, WI Foreign: None VA/DOD: None
Recall numberProduct, codes & lotsQuantity
F-1093-2016GERBER Organic 2ND FOODS Pears, Carrots & Peas, 3.5 oz., film pouches, 6 pouches per display box/ 2 display boxes per case; Asst Ecom PK2 18 pc, 3.94 Lbs.; UPC: 15000074319 GERBER Organic 2ND FOODS¿ Pears, Carrots & Peas Batch 51945335XX manufactured July 13, 2105 Best By: July 12, 2016 Batch 51955335XX manufactured July 14, 2015 Best By: July 13, 201651945335XX: 7196 cases (86,353 pouches), 51955335XX: 3060 cases (36,840 pouches)
F-1094-2016GERBER Organic 2ND FOODS¿ Carrots, Apples & Mangoes, 3.5 oz., film pouches, 6 pouches per display box/ 2 display boxes per case, 9Pc AsstA CbPk 1.96 Lbs; Asst EcomPk1 18 pc, 3.94 Lbs.; 48 Pc 10.48 Lbs.; 4 x 3.5 oz.; UPC: 15000074395 GERBER Organic 2ND FOODS¿ Carrots, Apples & Mangoes, Batch 51955335XX manufactured July 14, 2015 Best By: July 13, 2016; Batch 51965335XX manufactured July 15, 2015 Best By: July 14, 201651955335XX: 2685 cases (26,592 pouches), 51965335XX: 734 cases (8,808 pouches)
Based on the official FDA remedy

What to do — step by step

  1. Check Batch Numbers

    Verify if your pouches match Batch 51945335XX or 51955335XX with the corresponding Best By dates of July 12, 2016, or July 13, 2016.

  2. Inspect Packaging

    Look for air holes in the film pouches which could indicate potential spoilage from mold and yeast growth.

Where it went and when

Where it was distributed

Distributed in 36 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: yesNVWyoming: not listedWYSouth Dakota: not listedSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: not listedUTColorado: yesCONebraska: not listedNEMissouri: yesMOKentucky: yesKYWest Virginia: not listedWVVirginia: yesVAMaryland: yesMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Domestic: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, NC, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, VA, WA, WI Foreign: None VA/DOD: None” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Arizona, Arkansas, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maryland, Michigan, Minnesota, Mississippi, Missouri, Nevada, New Hampshire, New Jersey, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Washington, Wisconsin.

Recall timeline

FDA terminated this recall 11 months after the firm started it.

1. Firm started the recall: Mar 24, 201612. FDA classified it Class II: Apr 20, 201623. Published in FDA’s Enforcement Report: Apr 27, 201634. FDA terminated the recall: Feb 22, 2017420162017
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1093-2016 (March 24, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1093-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA