UnratedFood recall · FDA · Published April 12, 2024
Hiland Vitamin D Whole Milk Recall: May Contain Potable Water
Hiland Dairy Foods Company recalls Vitamin D Whole Milk products that may contain potable water. Consumers should check labels for specific batch numbers and use by dates to determine if affected.
“Hiland Vitamin D Whole Milk Recall: May Contain Potable Water.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/9455-hiland-vitamin-d-whole-milk-recall-may-contain-potable-water. Based on FDA recall #F-1241-2024 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1241-2024%22&limit=1).
Hiland Dairy Foods Company, LLC voluntarily recalled Vitamin D Whole Milk products distributed in Kansas and Missouri after they may contain potable water, the FDA said on April 12, 2024.
How to tell if you have it
Country Club, Price Chopper, Good & Gather, Hiland, Belfonte, Great Value, Hen House Vitamin D Whole Milk, 1 gallon
Country Club, Price Chopper, Good & Gather, Best Choice, Good Nature Family Farms Vitamin D Whole Milk, Half Gallon
Belfonte, Hiland Vitamin D Whole Milk, Quart
The hazard
The recalled milk may contain potable water. The FDA classified the recall as Class III.
Context
GovInfoNow's records show Hiland Dairy Foods Company, LLC has had five other recalls since January 11, 2018. Other recent recalls of similar products include Prairie Farms Fat Free Milk Recall (November 25, 2025), Lone Star Dairy Spray Dried Dairy Powder Recall (March 11, 2026), and California Dairies Low Heat Non-Fat Dried Milk Powder Recall (April 20, 2026).
How to tell if you have this one
Check for products labeled 'Hiland Vitamin D Whole Milk' with a 'Best If Use By' date of 04/18/24. Look for batch numbers 29-162A, 29-162, or 29-162 (as listed in the recall notice).
Brand
Hiland
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Labels
Look for the 'Best If Use By' date of 04/18/24 and batch numbers 29-162A, 29-162, or 29-162 on the milk container.
Where it went and when
Where it was distributed
Distributed in Kansas and Missouri.
Listed by the agency
Not listed
FDA distribution: “KS and MO” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Kansas, Missouri.
Recall timeline
FDA terminated this recall 17 months after the firm started it.
1Firm started the recall
2FDA classified it Class III
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-1241-2024 (April 12, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1241-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.