Recall record at a glance
| Official record | F-1622-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Talking Rain Beverage Co Inc. |
| Report date | Jul 18, 2018 |
| Recall initiation date | Jun 22, 2018 |
| Quantity | 684,977 cases (single pack = 214,311 cases and variety pack = 470,666 cases) |
| Location | Preston, WA, United States |
Official product description
Sparkling ICE Cherry Limeade Naturally Flavored Sparking Water, packaged in a PET bottles with a plastic cap, Net Wt. 17 ounces (502.8 ml). UPC code on bottle: 0 16571 95084 2. UPC on Single Pack Wrapper (1 flavor/12 bottles): 016571953126 UPC on Single Pack Wrapper (1 flavor/24 bottles): NONE ****************************************************************************************** Sparkling ICE Cherry Limeade is also assembled and sold in Variety Packs with other flavors (those other flavors are not affected by this recall). The UPCs on those Variety Packs are: 016571953614 (4 flavors/6 bottles of Sparkling ICE Cherry Limeade/24 bottles total). 016571950927 (4 flavors/3 bottles of Sparkling ICE Cherry Limeade/12 bottles total). 016571951283 (3 flavors/6 bottles of Sparkling ICE Cherry Limeade/18 bottles total . 016571950866 (UPC on Pallets of variety packs).
Why the product was recalled
Sparkling ICE Cherry Limeade, 17 oz. bottles, is recalled after the firm received a small number of customer complaints that reported an off-taste and off-odor of the product.
Distribution information
Distributed in AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, ME, MI, MN, MO, MS, NC, ND, NE, NJ, NM, NV, OH, OK, SC, SD, TN, TX, UT, VA, WA, and WI.
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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