Borden Dairy recalls Vitamin D milk with 1006 IU per quart, exceeding the labeled 400 IU. Consumers should check product details and contact Borden for guidance.
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.
Borden Dairy is recalling Vitamin D milk that contains more than double the labeled amount of Vitamin D (1006 IU per quart vs. 400 IU). This could lead to excessive Vitamin D intake, though the recall does not mention serious health risks.
The milk contains 1006 IU of Vitamin D per quart, which is more than double the labeled amount of 400 IU. While excessive Vitamin D can cause health issues, the recall does not indicate a risk of serious injury or death in normal use.
People who purchased Borden Vitamin D milk with the specified UPC codes and expiration dates between February 16-20, 2014 are likely affected. Those with sensitive health conditions or high Vitamin D needs may be at slightly higher risk.
Check for the product names and UPC codes listed in the recall notice. The milk was sold with expiration dates from February 16 to 20, 2014, and includes specific packaging sizes like quarts, gallons, and pints.
Review the product's UPC codes and expiration dates to confirm if it matches the recalled items.
The recall states the milk has more than double the labeled Vitamin D, but it does not mention serious health risks. The product is not considered dangerous in normal use.
Check the product's UPC codes and expiration dates listed in the recall notice, which range from February 16 to 20, 2014.
The recall does not specify a remedy, so contact Borden Dairy for guidance on next steps.
We’ve drafted a message you can send Borden to request your refund or repair — edit it as you like.
Subject: Recall F-1974-2014 — Borden Borden Hello, I own a Borden that is covered by recall F-1974-2014 from Borden. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
