Fresh Express Kit Salsa! Ensalada with condiments(toppings that include cheese), labeled…
Fresh Express Incorpated recalled this product and the FDA reported the enforcement action on 21 February 2024 as Class I. The recall was initiated by the firm. Product has the potential to be contaminated with Listeria monocytogenes. The condiment pack in the salad kit contains cheese recalled by the cheese supplier.
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
- Fresh Express Kit Salsa! Ensalada with condiments(toppings that include cheese), labeled salad bag (Iceberg & Romaine Lettuce, Salsa Ranch Dressing, Nacho Taco Seasoned Cheese Yellow & Blue Tortilla Strips), Net Wt 12.1 oz, 6 bags per case. UPC 071279309026
- UPC
- 071279309026
- Reason for recall
- Product has the potential to be contaminated with Listeria monocytogenes. The condiment pack in the salad kit contains cheese recalled by the cheese supplier.
- Recalling firm
- Fresh Express Incorpated
- Firm location
- Windermere, Florida, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-0876-2024
- Quantity
- 4826 Cases
- Distribution
- AL, FL, GA, CA, UT, WA; Canada
- Initiated
- 8 February 2024
- Reported by FDA
- 21 February 2024
- Terminated
- 16 April 2024
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- Lot Number:S002, S003, S005, S008, S009, S012, S015, S019, S023, S026, S030, S033, S353, S356, S361, S362, S364 Expiration/Use By Date : 01/06/2024, 01/10/2024, 01/15/2024, 01/16/2024, 01/18/2024, 01/21/2024, 01/22/2024, 01/24/2024, 01/27/2024, 01/28/2024, 01/31/2024, 02/3/2024 , 02/07/2024, 02/11/2024 , 02/14/2024, 02/18/2024, 02/20/2024 Condiment Pack Use-by Dates 02/28/2024 to 04/04/2024
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. 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 2 of them.
- The recall ran for 2 months, from 8 February 2024 to termination on 16 April 2024. 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 6 states, and the FDA published the enforcement report 13 days 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.
Named in the distribution pattern: Alabama, Florida, Georgia, California, Utah, Washington. 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 cheese, fresh produce, bakery and sauces, dips and condiments. A product can sit in more than one.
Other cheese 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 Fresh Express Incorpated
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 16 other records name this firm.
All 17 records for Fresh Express Incorpated
All 2024 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.