Creative Snacks Co. Sunny Day Splendor, 10 lb. bulk, UPC 816512014653; Creative Snacks…
Creative Snacks Co., LLC recalled this product and the FDA reported the enforcement action on 10 August 2016 as Class I. The recall was initiated by the firm. Potential presence of Listeria Monocytogenes
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
- Creative Snacks Co. Sunny Day Splendor, 10 lb. bulk, UPC 816512014653; Creative Snacks Co. Sunny Day Splendor 10 oz. cup, UPC 816512010983
- UPC
- 816512014653
- Reason for recall
- Potential presence of Listeria Monocytogenes
- Recalling firm
- Creative Snacks Co., LLC
- Firm location
- Greensboro, North Carolina, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-1866-2016
- Quantity
- 90 cases
- Distribution
- CA, CT, DE, GA, IN, ME, MA, MN, NJ, NY, NC, SC, TX, UT
- Initiated
- 5 May 2016
- Reported by FDA
- 10 August 2016
- Terminated
- 18 July 2017
- Firm notified by
- Telephone
- Product codes
- Creative Snacks 10 lb. bulk 1192031716; Creative Snacks 10 oz. cup 2930041916
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. 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 is one of 7 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 7 separate recalls, which almost every published figure does, overstates it by a factor of 7. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 7 of them.
- The recall ran for 14 months, from 5 May 2016 to termination on 18 July 2017. 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 3 months after the firm began the recall.
- Recalls of a snack or confectionery product run a median of 7 months, so this one was longer than usual for its category. Snacks and confectionery recall for allergens more than for anything else, because a chocolate or a coated snack passes through shared equipment carrying milk, soy and nuts, and the label is the only control between them and the consumer.
Named in the distribution pattern: California, Connecticut, Delaware, Georgia, Indiana, Maine, Massachusetts, Minnesota, New Jersey, New York, North Carolina, South Carolina, Texas, Utah. 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
Listeria monocytogenes
Listeria monocytogenes is a bacterium that grows at refrigeration temperature, which is why it dominates recalls of ready-to-eat foods that are never cooked again before they are eaten.
A preventive controls plan covers Listeria contamination 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)(3)
- Sanitation controls: the controls on cleaning food-contact surfaces and on preventing cross-contact and cross-contamination from insanitary objects, people and equipment.
- 21 CFR 117.165(a)(3)
- Environmental monitoring: testing the processing environment for an environmental pathogen, required when a ready-to-eat food is exposed to the environment before packaging.
- 21 CFR 117.150
- Corrective actions: what a facility does when a preventive control was not properly implemented, including identifying and correcting the problem and evaluating the food for safety.
Filed under snacks and confectionery. A product can sit in more than one.
Other snacks and confectionery 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 Creative Snacks Co., LLC
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 8 other records name this firm.
All 9 records for Creative Snacks Co., LLC
All 2016 recalls · All FDA food recall data
21 CFR 117.135(c)(3) 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.