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Lower risk Food recall · FDA · Published September 13, 2019

Abbott Calcilo XD Infant Formula Recall: Off-color and Odor Risk

Abbott recalls low-calcium vitamin D-free infant formula with iron powder in 13.2 oz cans due to off-color and odor from compromised can seams.

🇺🇸 FDA recall #F-0022-2020FoodAbbott Laboratories ›
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Recalling firmAbbott Laboratories100 Abbott Park Rd Bldg Ap8b · Abbott Park, IL 60064-3502
✎ GovInfoNow plain-language explainer

Abbott is recalling low-calcium vitamin D-free infant formula with iron powder in 13.:2 oz cans. The product may have off-color and odor due to a compromised can seam that could allow air in. Read more at govinfonow.com/recall/16655-abbott-calcilo-xd-infant-formula-recall-off-color-and-odor.

Source Summary by GovInfoNow · govinfonow.com/recall/16655-abbott-calcilo-xd-infant-formula-recall-off-color-and-odor · Updated October 5, 2026 · FDA enforcement record: FDA #F-0022-2020

Cite this page

“Abbott Calcilo XD Infant Formula Recall: Off-color and Odor Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16655-abbott-calcilo-xd-infant-formula-recall-off-color-and-odor. Based on FDA recall #F-0022-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0022-2020%22&limit=1).

The FDA announced on 2019-09-13 that Abbott Laboratories recalled Abbott Calcilo XD infant formula due to off color and odor caused by a compromised can seam. The agency mandated the Class II recall of 2,922 cans distributed nationwide in the U.S., Canada, and Malaysia.

How to tell if you have it

  • Brand: Abbott Laboratories
  • Product: Abbott Calcilo XD, Low-calcium Vitamin D-Free Infant formula with iron
  • Form: Powder in a 13.2 oz. can
  • Packaging: 6 cans per case
  • Lot number: 79696K80

The hazard

The recall addresses off color and odor resulting from a compromised can seam due to product powder in the seam. This poor seal potentially allowed air into the container.

Context

GovInfoNow's records show Abbott Laboratories has issued 33 other recalls since 2012-05-14. Recent brand recalls include a 2025-11-13 correction for potential performance issues in the Alinity ci-series System Control Module and a 2025-09-18 software issue affecting Abbott Alinity hq Analyzer results. Other recent recalls of similar products include a2 Platinum Premium Infant Formula Recall (2026-05-01), Preema Food Color Powder Recall (2026-01-29), and Nara Organics Infant Formula Recall (2026-06-13).

How to tell if you have this one

Check for off-color or odor in the 13.2 oz cans with lot number 79696K80. The product is sold in cases of 6 cans.

  • Brand
    Abbott Laboratories
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check for Off-Color or Odor

    Inspect the formula for off-color or odor before use.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide in the US. Canada and Malaysia.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 8 months after the firm started it.

1. Firm started the recall: Sep 13, 201912. FDA classified it Class II: Oct 8, 201923. Published in FDA’s Enforcement Report: Oct 16, 201934. FDA terminated the recall: Apr 30, 2020420192020
  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-0022-2020 (September 13, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0022-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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