Recall record at a glance
| Official record | F-0062-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | McCain Foods USA |
| Report date | Oct 29, 2014 |
| Recall initiation date | Sep 10, 2014 |
| Quantity | (1) Lot no. 1000843118 - 748 cases, and (2) Lot no. 1000843114 - 264 cases, and (3) Lot no. V40728 - 2109 cases |
| Location | Lisle, IL, United States |
Official product description
Frozen battered onion rings packaged in 40 oz plastic bags, 6/case under the following private labels: (1) Imperial Sysco 3/8" Battered Onion Rings, Distributed by Sysco Corporation, Houston, Texas 77077-2099, Product no.: 41010044, and UPC code: 074865 84822 0; and (2) KickStarts Batter Dipt Onion Rings, Net Wt. 40 oz (2.5 lb), Distributed by Food Services of America, Inc., Seattle, WA 98106, Product no. 10210070, UPC 0 41493 49025 0; and (3) McCain Onion Rings, Net Wt. 3.18 kg, packaged as 8 x 397g boxes, Product of U.S.A., Prepared for: McCain Foods (Canada) A Division of McCain Foods Limited, Florenceville-Bristol, New Brunswick, Canada E7L 1B2, Product No. 1000001362, UPC 0 55773 00089 4.
Why the product was recalled
Product may be contaminated with glass.
Distribution information
Distribution was to foodservice customers in AZ, CA, CO, GA, IA, IL, LA, MN, MO MT, ND, NE, NM, PA, TN, TX, WA, and WI. Product was distributed in 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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