KRAFT SINGLES AMERICAN CHEESE SLICES - 16OZ/24CT UPC:2100061526
C & S Wholesale Grocers, Inc. recalled this product and the FDA reported the enforcement action on 31 July 2019 as Class II. The recall was initiated by the firm. Products were not held at an appropriate temperature due to a mechanical malfunction during transportation.

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
- KRAFT SINGLES AMERICAN CHEESE SLICES - 16OZ/24CT UPC:2100061526
- UPC
- 2100061526
- Reason for recall
- Products were not held at an appropriate temperature due to a mechanical malfunction during transportation.
- Recalling firm
- C & S Wholesale Grocers, Inc.
- Firm location
- Westfield, Massachusetts, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-1799-2019
- Quantity
- unknown
- Distribution
- Two Target Stores 1. 98 Veterans Memorial Highway in Commack, New York 2. 160 North Research Place in Central Islip, New York
- Initiated
- 17 June 2019
- Reported by FDA
- 31 July 2019
- Terminated
- 31 July 2019
- Firm notified by
- Telephone
- Product codes
- Exact codes are unknown. The product being recalled was sold on June 17, 2019 at Target Stores in Commack, NY and Central Islip, NY.
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 is one of 330 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 330 separate recalls, which almost every published figure does, overstates it by a factor of 330. 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 330 of them.
- The recall ran for 6 weeks, from 17 June 2019 to termination on 31 July 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.
- Recalls of cheese run a median of 7 months, so this one was shorter than usual for its category. Cheese dominates Listeria recalls among dairy products because soft and semi-soft varieties hold enough moisture for the organism to grow at refrigeration temperature, and because most are eaten without any further cooking step.
Filed under cheese. A product can sit in more than one.
Other cheese 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 C & S Wholesale Grocers, Inc.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 337 other records name this firm.
All 338 records for C & S Wholesale Grocers, Inc.
All 2019 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.