Food recall

Nutricia North America recall: Nutricia KetcoCal 4:1 LQ Unflavored in 237ml (8fl oz) packaged in tetra prisma paper aseptic carton - 3 cartons per...

Nutricia North America, of Rockville, MD, recalled Nutricia KetcoCal 4:1 LQ Unflavored in 237ml (8fl oz) packaged in tetra prisma paper aseptic carton - 3 cartons per.... The FDA's reason: “Incorrect product in packaging.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on October 20, 2023, and the FDA first listed it in its Enforcement Report of November 15, 2023. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

Labeling, packaging or manufacturing problems

Status

Terminated

Closed September 18, 2024

The recall

Company
Nutricia North America (Rockville, MD)
Reason, in FDA's words
“Incorrect product in packaging”
Where it was sold
247 kits shipped within US (Alabama, California, Colorado, Illinois, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, New Hampshire, New Jersey, New Mexico, New York, Ohio, Pennsylvania, Rhode Island, South Carolina, Texas, Virginia, Washington, Wisconsin) 36 kits shipped within Canada (Ontario, Quebec, Prince Edward, British Columbia, Alberta)
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
93288

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-0406-2024 Class II

    Nutricia KetcoCal 4:1 LQ Unflavored in 237ml (8fl oz) packaged in tetra prisma paper aseptic carton - 3 cartons per box *Sample Kits*

    Codes: Expiration: DEC 10 2023 Batch/Lot 2023.12.10

    Quantity: 283 kits

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of November 15, 2023.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.