Inspired Organic Sunflower Butter 16oz. plastic jar, 6 per case UPC #: 863669742526…
Lipari Foods Operating Company, LLC recalled this product and the FDA reported the enforcement action on 26 December 2018 as Class I. The recall was initiated by the firm. Product testing returned positive test results for 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
- Inspired Organic Sunflower Butter 16oz. plastic jar, 6 per case UPC #: 863669742526 refrigerate after opening
- UPC
- 863669742526
- Reason for recall
- Product testing returned positive test results for Listeria monocytogenes.
- Recalling firm
- Lipari Foods Operating Company, LLC
- Firm location
- Warren, Michigan, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-0775-2019
- Quantity
- 972 cases
- Distribution
- FL, IA, IL, IN, KY, MD, MI, MN, MO, NY, OH, PA, TN, WI, WV, CANADA
- Initiated
- 11 December 2018
- Reported by FDA
- 26 December 2018
- Terminated
- 20 May 2019
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- All Lots All Dates Item number 967064
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 4 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 4 separate recalls, which almost every published figure does, overstates it by a factor of 4. All 4 of them are listed on this page.
- The recall ran for 5 months, from 11 December 2018 to termination on 20 May 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 distribution pattern names 15 states, and the FDA published the enforcement report 2 weeks after the firm began the recall.
- Recalls of milk or a dairy product run a median of 7 months, so this one was about typical for its category. Dairy recalls split between pathogen contamination in products that skipped or under-ran pasteurisation and undeclared milk in products that should never have contained it, which is the same allergen viewed from two directions.
Named in the distribution pattern: Florida, Iowa, Illinois, Indiana, Kentucky, Maryland, Michigan, Minnesota, Missouri, New York, Ohio, Pennsylvania, Tennessee, Wisconsin, West Virginia. 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 milk and dairy. A product can sit in more than one.
Every product in this recall
The FDA opened 4 enforcement records for this one recall, one per product code. This page carries all of them; the 3 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 |
|---|---|---|---|---|
| 2018-12-26 | Inspired Organic Tahini Butter 16oz. plastic jar, 6 per case UPC #: 863669742564 refrigerate after opening | Lipari Foods Operating Company, LLC | Product testing returned positive test results for Listeria monocytogenes. | Class I |
| 2018-12-26 | Inspired Organic Peanut Butter 16oz. plastic jar, 6 per case UPC #: 863669742588 refrigerate after opening | Lipari Foods Operating Company, LLC | Product testing returned positive test results for Listeria monocytogenes. | Class I |
| 2018-12-26 | Inspired Organic Almond Butter 16oz. plastic jar, 6 per case UPC #: 863669742540 refrigerate after opening | Lipari Foods Operating Company, LLC | Product testing returned positive test results for Listeria monocytogenes. | Class I |
Other milk and dairy 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 Lipari Foods Operating Company, LLC
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 54 other records name this firm.
All 55 records for Lipari Foods Operating Company, LLC.
All 2018 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.