16 count Smartfood Delight Variety Pack Sack
Frito-Lay, Inc. recalled this product and the FDA reported the enforcement action on 12 December 2018 as Class I. The recall was initiated by the firm. The firm is recalling 1/2 oz. bags of Smartfood Delight Sea Salt Flavored popcorn packaged in two variety pack offerings. The popcorn bags have the potential to contain cheese-flavored chips and therefore undeclared milk.
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
- 16 count Smartfood Delight Variety Pack Sack
- Reason for recall
- The firm is recalling 1/2 oz. bags of Smartfood Delight Sea Salt Flavored popcorn packaged in two variety pack offerings. The popcorn bags have the potential to contain cheese-flavored chips and therefore undeclared milk.
- Recalling firm
- Frito-Lay, Inc.
- Firm location
- Plano, Texas, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-0689-2019
- Quantity
- 19,565 sacks (total)
- Distribution
- Alabama, Arkansas, Colorado, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Mexico, Ohio, Oklahoma, South Carolina, South Dakota, Tennessee, Texas, Virginia, Wisconsin, West Virginia and Wyoming.
- Initiated
- 2 November 2018
- Reported by FDA
- 12 December 2018
- Terminated
- 5 February 2019
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- use by dates of 4 DEC 2018 OR 18 DEC 2018, and 11-digit manufacturing code that will include the letter combination AM in the second and third position (example: xAMxxxxxxxx)
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 2 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 2 separate recalls, which almost every published figure does, overstates it by a factor of 2. All 2 of them are listed on this page.
- The recall ran for 3 months, from 2 November 2018 to termination on 5 February 2019. 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 FDA published the enforcement report 6 weeks after the firm began the recall.
- The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.
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.
The allergens named in this record: milk.
Every product in this recall
The FDA opened 2 enforcement records for this one recall, one per product code. This page carries all of them; the 1 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2018-12-12 | 16 count Crunch & Pop Mix Variety Pack Sack | Frito-Lay, Inc. | The firm is recalling 1/2 oz. bags of Smartfood Delight Sea Salt Flavored popcorn packaged in two variety pack offerings. The popcorn bags have the potential to contain cheese-flavored chips and therefore undeclared milk. | Class I |
Other records from Frito-Lay, Inc.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 41 other records name this firm.
All 42 records for Frito-Lay, Inc.
All 2018 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.