FDA recall record

Nutricia KetcoCal 4:1 LQ Unflavored in 237ml recall — FDA F-0406-2024

Incorrect product in packaging

Class IIclassification
F-0406-2024official record ID
Nov 15, 2023report date

Recall record at a glance

Official recordF-0406-2024
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNutricia North America
Report dateNov 15, 2023
Recall initiation dateOct 20, 2023
Quantity283 kits
LocationRockville, MD, United States

Official product description

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

Why the product was recalled

Incorrect product in packaging

Distribution information

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)

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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