Ukrop's Homestyle Foods LLC recalled this product and the FDA reported the enforcement action on 11 June 2025 as Class I. The recall was initiated by the firm. Salmonella. The firm received cucumbers produced by Bedner Farms.
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
Ukrop's Marinated Cucumber Salad INGREDIENTS: Cucumber, distilled vinegar***apple cider vinegar, sugar, red onion, water, canola oil***NET WT 16 OZ (1LB/454g) UPC 7 22515 24902 5; NET WT 36 OZ (2.25LB/1.02kg) UPC 7 22515 25224 7; NET WT 5LB (2.27kg) UPC 7 22515 29354 7 Ukrop's Homestyle Foods, LLC Richmond, VA 23230
UPC
722515249025
Reason for recall
Salmonella. The firm received cucumbers produced by Bedner Farms.
Product was shipped to the following states: KY, NC, OH, VA & WV.
Initiated
21 May 2025
Reported by FDA
11 June 2025
Firm notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product codes
16 oz: Sell By Dates: 5/11/25 through 5/26/25 36 oz: Sell By Dates: 5/11/25 through 5/26/25 5 lb: Sell By Dates: 5/11/25 through 5/26/25
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.
This recall has no termination date on the record, so as published it had not been terminated under 21 CFR 7.55.
The distribution pattern names 2 states, and the FDA published the enforcement report 3 weeks after the firm began the recall.
Fresh produce is the category where contamination arrives before the facility does: irrigation water, soil amendments and field workers are the routes, and nothing downstream of the farm is a kill step for a product eaten raw.
Named in the distribution pattern: North Carolina, Ohio. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
Salmonella is a bacterium that survives in low-moisture foods for months, which is why it appears in recalls of products that carry no water for it to grow in: nut butters, spices, flour and dry pet food.
A preventive controls plan covers Salmonella 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)(1)
Process controls: the controls that apply a treatment, such as a validated kill step, at the point where it reduces the hazard to a safe level.
21 CFR 117 subpart G
Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
21 CFR 117.165(a)(2)
Product testing: testing as a verification activity, appropriate to the facility, the food and the nature of the preventive control.
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.
21 CFR 117.135(c)(1) 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.
Recall 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.
