RECALL RECORD — CLASS IIIRecall closedF-1974-2014/FDA enforcement

Vitamin D Milk Grade a Pasteurized Homogenized

What you need to know

Class III
  • What happened

    The firm was informed that the product has more than double the labeled amount of Vitamin D. The target minimum level is 400 IU per Qt. The product contains 1006 IU per Qt.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDAIN, KY, OH, WVMore food

Advertisement

Ad

Know someone who bought this?

A quick share can keep a pantry check from becoming a missed warning.

Match before you discard

Product identification

Source: FDA FOOD

Brand nameBorden Dairy Co of Cincinnati LLC
Recalling firmBorden Dairy Co of Cincinnati LLCCincinnati, OH, United States
UPC / barcodes
0 72000 15233 10 72000 15238 60 70554 27197 90 72804 00190 30 72804 00158 30 72804 00159 00 41498 19215 07 58108 22723 17 58108 22724 80 41270 02491 40 41270 05844 50 80761 03000 3
Lot / date codes
  • IMS # 39-112
  • exp dates: 2/16/14, 2/17/14, 2/18/14, 2/19/14, 2/20/14.
Distribution area
INKYOHWV

The product was shipped to the following states: IN, KY, OH & WV.

United States

Quantity affected30/300 gal totes, 13, 457cs/4/1 gal ctn, 51.44cs/9/¿ gal ctn, 45cs/12/1 qt ctn, 221.75cs/20/1 pt ctn, 31.18cs/50/¿ pt ctn, & 8/5gal bags.
Recall initiationFDA report date: June 4, 2014
FDA recall numberF-1974-2014

Beyond the headline

The recall, in context

Borden Dairy Co of Cincinnati LLC initiated this food recall on February 6, 2014. The FDA enforcement report states: The firm was informed that the product has more than double the labeled amount of Vitamin D. The target minimum level is 400 IU per Qt. The product contains 1006 IU per Qt. The FDA report lists distribution as: The product was shipped to the following states: IN, KY, OH & WV.

The FDA enforcement report describes the reason as: The firm was informed that the product has more than double the labeled amount of Vitamin D. The target minimum level is 400 IU per Qt. The product contains 1006 IU per Qt.

Vitamin D Milk Grade a Pasteurized Homogenized was made or distributed by Borden Dairy Co of Cincinnati LLC in Cincinnati, OH, United States. This page reflects FDA report F-1974-2014, dated June 4, 2014.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Vitamin D Milk Grade a Pasteurized Homogenized recall?

Borden Dairy Co of Cincinnati LLC recalled Vitamin D Milk Grade a Pasteurized Homogenized in an FDA Class III enforcement action reported as F-1974-2014. The firm was informed that the product has more than double the labeled amount of Vitamin D. The target minimum level is 400 IU per Qt. The product contains 1006 IU per Qt.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Borden Dairy Co of Cincinnati LLC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1974-2014. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Related alerts

Recent Other safety concern recalls

All alerts

Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.