Recall record at a glance
| Official record | F-0298-2013 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Oregon Ice Cream, LLC |
| Report date | Oct 24, 2012 |
| Recall initiation date | Sep 20, 2012 |
| Quantity | 1400 cases/3 cups |
| Location | Eugene, OR, United States |
Official product description
Alden's Cookies and Cream is an ice cream product. It is packaged in a 1.5 quart (48 oz) cup. The LID of the recalled product is labeled in parts:"***ORGANIC***Alden's ICE CREAM***COOKIES 'n CREAM***1.5 QTS (1.42L)***". The CUP of the recalled product is labeled in parts: "***ORGANIC***Alden's ICE CREAM***CHOLOCATE CHOCOLATE CHIP***MFD. BY OREGON ICE CREAM***EUGENE, OR 97402***1-800-282-2202***www.aldensicecream.com***". The INGREDIENTS' STATEMENT on the cup is labeled in parts: "***ORGANIC MILK AND CREAM, ORGANIC EVAPORATED CANE JUICE, ORGANIC CHOCOLATE LIQUOR AND COCOA BUTTER, ORGANIC ALKALIZED COCOA, ORGANIC TAPIOCA SYRUP, ORGANIC PALM KERNEL OIL, ORGANIC VANILLA EXTRACTS, ORGANIC TAPIOCA STARCH, NON-GMO SOY LECITHIN, GUAR GUM, LOCUST BEAN GUM, XANTHAN GUM***".
Why the product was recalled
Alden's Cookies and Cream was packaged in the wrong cup and a correct lid was used, but wheat was not declared on the finished product's label.
Distribution information
Product was distributed to distribution centers in CA, CO, CT, IA, IN, NH, and PA.
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
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