Recall record at a glance
| Official record | F-2187-2014 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | NW Nutritional Foods LLC |
| Report date | Jul 23, 2014 |
| Recall initiation date | Mar 27, 2014 |
| Quantity | 50,904 bars |
| Location | Seattle, WA, United States |
Official product description
There are three different labels for this product. Label #1 individual bar 100% Natural Zing Nutrition Bar, DARK CHOCOLATE SUNFLOWER MINT, Gluten Free & Vegan, NET WT. 1.76 OZ. (50g), Manufactured For: Zing Bars Seattle, WA 98125. Label #1 display Carton 100% Natural Zing Nutrition Bar, Gluten Free & Vegan, DARK CHOCOLATE SUNFLOWER MINT, 12/1.76 OZ(50g) Bars, NET WT. 1 LB 5.12 OZ. (600g). Label #2 individual bar 100% Natural Zing Nutrition Bar, NUT FREE DARK CHOCOLATE SUNFLOWER MINT, Gluten Free & Vegan, NET WT. 1.76 OZ. (50g), Manufactured For: Zing Bars Seattle, WA 98125. Label #3 individual bar 100% Natural Zing Nutrition Bar, NUT FREE DARK CHOCOLATE MINT, Gluten Free, Vegan & Non GMO, NET WT. 1.76 OZ. (50g), Manufactured For: Zing Bars Seattle, WA 98125. Chocolate covered nutrition bar packaged in 2 layer metallized BOPP film, 1.76 oz each. 12 individually wrapped bars per display box. Bar UPC code: 8 55531 00206 7; Display Box UPC code: 8 55531 00213 5; Master Case UPC code: 1 08 55531 00213 2.
Why the product was recalled
Undeclared milk found in bars labeled "dairy free" or "vegan."
Distribution information
Product was distributed in US to AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO,MMS, MT, NC, ND, NE, NH, NJ, NM, NV, OH, OK, OR, PA, RI, SC, SD, TN, TX, VT, VA, VT, WA, AND WI. Product was distributed outside the US to British Columbia, Ontario and Quebec, Canada.
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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