Clear American brand "Strawberry Punch Snow Cone" flavored sparkling water beverage with…
Refresco Beverages US Inc recalled this product and the FDA reported the enforcement action on 17 August 2022 as Class II. The recall was initiated by the firm. The product may contain trace amounts of coconut, which is not declared on the labeling. Laboratory analysis was unable to detect any coconut allergen, however the firm has decided to recall out of an abundance of caution.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Clear American brand "Strawberry Punch Snow Cone" flavored sparkling water beverage with other natural flavors; 1-liter clear plastic bottles. Best if Used by dates in August-October 2022.
- Reason for recall
- The product may contain trace amounts of coconut, which is not declared on the labeling. Laboratory analysis was unable to detect any coconut allergen, however the firm has decided to recall out of an abundance of caution.
- Recalling firm
- Refresco Beverages US Inc
- Firm location
- Tampa, Florida, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-1538-2022
- Quantity
- 87, 859 cases (12 one-liter bottles per case)
- Distribution
- Stores throughout AZ, CA, IL, IN, KY, ME, NV, NY, OH, PA, SC, UT, VA, WA, WI
- Initiated
- 7 July 2022
- Reported by FDA
- 17 August 2022
- Terminated
- 20 October 2022
- Firm notified by
- Product codes
- BEST IF USED BY Aug 01 22 BEST IF USED BY Aug 04 22 BEST IF USED BY Aug 05 22 BEST IF USED BY Aug 16 22 BEST IF USED BY Aug 17 22 BEST IF USED BY Aug 18 22 BEST IF USED BY Aug 22 22 BEST IF USED BY Aug 29 22 BEST IF USED BY Sep 03 22 BEST IF USED BY Sep 09 22 BEST IF USED BY Sep 14 22 BEST IF USED BY Sep 15 22 BEST IF USED BY Sep 29 22 BEST IF USED BY Sep 30 22 BEST IF USED BY Oct 06 22 BEST IF USED BY Oct 08 22 BEST IF USED BY Oct 11 22 BEST IF USED BY Oct 17 22 BEST IF USED BY Oct 20 22 BEST IF USED BY Oct 23 22
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This record is the only one the FDA opened for its recall event, so it covers a single product code.
- The recall ran for 3 months, from 7 July 2022 to termination on 20 October 2022. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 14 states, and the FDA published the enforcement report 6 weeks after the firm began the recall.
- Recalls of fresh produce run a median of 7 months, so this one was shorter than usual for its category. Fresh produce is the category where contamination arrives before the facility does: irrigation water, soil amendments and field workers are the routes, and nothing downstream of the farm is a kill step for a product eaten raw.
Named in the distribution pattern: California, Illinois, Indiana, Kentucky, Maine, Nevada, New York, Ohio, Pennsylvania, South Carolina, Utah, Virginia, Washington, Wisconsin. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Undeclared allergens
An undeclared allergen recall means a food contained one of the major allergens and the label did not say so, either because the wrong label was applied or because an ingredient carried an allergen nobody traced.
A preventive controls plan covers an undeclared allergen under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.135(c)(2)
- Food allergen controls: the written preventive controls that keep an allergen out of a food it does not belong in, and that get the allergens present onto the label.
- 21 CFR 101.4
- Ingredient declaration: every ingredient listed by its common name, in descending order of predominance, on the label of a packaged food.
- 21 CFR 117 subpart G
- Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
Filed under fresh produce and beverages and juice. A product can sit in more than one.
Other fresh produce recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Refresco Beverages US Inc
The FDA opens one enforcement record per product code, so several of these are frequently one recall event.
All 3 records for Refresco Beverages US Inc
All 2022 recalls · All FDA food recall data
21 CFR 117.135(c)(2) is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.