Backcountry Dried Apricots 9ounce plastic bag 12 packages per case
Lipari Foods Operating Company, LLC. recalled this product and the FDA reported the enforcement action on 4 August 2021 as Class I. The recall was initiated by the firm. Sulfites not disclosed on labeling
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
- Backcountry Dried Apricots 9ounce plastic bag 12 packages per case
- Reason for recall
- Sulfites not disclosed on labeling
- Recalling firm
- Lipari Foods Operating Company, LLC.
- Firm location
- Warren, Michigan, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-0795-2021
- Quantity
- 86 cases
- Distribution
- Distributed to retail locations in the following states: AL, FL, GA, ID, IL, IN, KS, KY, MI, MO, NC, OH, PA, TN, UT, VA, WI WV.
- Initiated
- 16 July 2021
- Reported by FDA
- 4 August 2021
- Terminated
- 23 September 2021
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- Best By Dates: 07/2021, 11/2021, 12/2021 Lot No. 440021117 Product No. 276033
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 record is the only one the FDA opened for its recall event, so it covers a single product code.
- The recall ran for 2 months, from 16 July 2021 to termination on 23 September 2021. 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 3 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.
Named in the distribution pattern: Florida, Georgia, Idaho, Illinois, Indiana, Kansas, Kentucky, Michigan, Missouri, North Carolina, Ohio, Pennsylvania, Tennessee, Utah, Virginia. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
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 2021 recalls · All FDA food recall data
Behind every recall is a clause 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.