Recall record at a glance
| Official record | F-1974-2014 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Terminated |
| Recalling firm | Borden Dairy Co Of Cincinnati LLC |
| Report date | Jun 4, 2014 |
| Recall initiation date | Feb 6, 2014 |
| Quantity | 30/300 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. |
| Location | Cincinnati, OH, United States |
Official product description
Vitamin D Milk GRADE A PASTEURIZED HOMOGENIZED; 4-oz paper, 300-gal totes, Gallons, 1/2 gallons, pints, quarts, paper 1/2 pints, 5-gal dispense bags. INGREDIENTS: MILK AND VITAMIN D3. Product is sold under the following brand names and UPC codes: American Fare: Gal: 0 72000 15233 1, ¿ Gal: 0 72000 15238 6; Community Market: Gal: 0 70554 27197 9; Dairymens: Gal: 0 72804 00190 3, ¿ Gal: 0 72804 00158 3 & Pint: 0 72804 00159 0; Friendly Farms: Gal: 0 41498 19215 0; Glenview Farms: Gal: 7 58108 22723 1, 1/2Pt: 7 58108 22724 8; IGA: Gal: 0 41270 02491 4 & ¿ Gal: 0 41270 05844 5; Modern Foods: Gal: 0 80761 03000 3; Our Family: Gal: 0 70253 65100 7; UDF: Gal: 0 76310 05005 9, ¿ Gal: 0 76310 05002 8, Qt: 0 76310 05300 5 & Pt: 0 76310 05250 3.
Why the product was recalled
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.
Distribution information
The product was shipped to the following states: IN, KY, OH & WV.
How to read the classification
FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement 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
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