Chicken flavored broth base and seasoning, low sodium sold under the Orrington Farms…
Kent Precision Foods Group, Inc. recalled this product and the FDA reported the enforcement action on 17 December 2014 as Class II. The recall was initiated by the firm. Orrington Farms Chicken Flavored Broth Base & Seasoning, Low Sodium labels were placed on jars of Orrington Farms Beef Flavored Broth Base & Seasoning, Low Sodium.

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
- Chicken flavored broth base and seasoning, low sodium sold under the Orrington Farms brand in 5 oz. plastic jars.
- Reason for recall
- Orrington Farms Chicken Flavored Broth Base & Seasoning, Low Sodium labels were placed on jars of Orrington Farms Beef Flavored Broth Base & Seasoning, Low Sodium.
- Recalling firm
- Kent Precision Foods Group, Inc.
- Firm location
- Bolingbrook, Illinois, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-0705-2015
- Quantity
- 13,572 jars
- Distribution
- US: Nationwide (AZ, IA, IL, IN, MA, MD, MI, MN, NE, NH, NJ, NV, NY, PA, SC, TN, WI)
- Initiated
- 27 October 2014
- Reported by FDA
- 17 December 2014
- Terminated
- 27 October 2015
- Firm notified by
- Letter
- Product codes
- Product Code: L334 12233. UPC: 0 72058 60864 4. Lot Number: B4036P. Best By: AUG 2015.
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 12 months, from 27 October 2014 to termination on 27 October 2015. 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 7 weeks after the firm began the recall.
- Recalls of meat or poultry run a median of 8 months, so this one was longer than usual for its category. Most meat and poultry is regulated by USDA FSIS rather than the FDA, so a product appearing in this FDA dataset is usually a closed-faced sandwich, a product with meat as a minor ingredient, or a food FSIS does not claim.
Named in the distribution pattern: Iowa, Illinois, Indiana, Massachusetts, Maryland, Michigan, Minnesota, Nebraska, New Hampshire, New Jersey, Nevada, New York, Pennsylvania, South Carolina, Tennessee. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
Filed under meat and poultry and spices and seasonings. A product can sit in more than one.
Other meat and poultry recalls
These are the closest records in the corpus: the same kind of food. 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 Kent Precision Foods Group, Inc.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event.
All 4 records for Kent Precision Foods Group, Inc.
All 2014 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.