Whole and Cut Cucumbers packaged in the following sizes: 1. Peak Cucumber Item 08027, 24 count. Product of Mexico.
Summary
The FDA issued a Class I for Whole and Cut Cucumbers packaged in the following sizes: 1. Peak Cucumber Ite by RUSS DAVIS WHOLESALE. Reason: Cucumbers have potential to be contaminated with Salmonella..
Details
Source
Food Recall
External ID
F-0367-2025
Action Date
2025-01-08
Status
Terminated
Category
food
Product Description
Whole and Cut Cucumbers packaged in the following sizes: 1. Peak Cucumber Item 08027, 24 count. Product of Mexico. 2. Peak Cucumber Item 08009, 5 LB. Product of Mexico. 3. Cucumber Super Select Item 22200, 24 count. Product of Mexico. 4. Cucumber Item 22201, 5 lb. Product of Mexico. 5. Cucumber Super Select Item 22227, 6 CT. Product of Mexico. 6. Cucumber 1/4" Slice/Skin-On Net Wt 5 LB. Keep Refrigerated. Mexico 7. Cucumber Diced 3/8" Net Wt. 5 LB. Keep Refrigerated. Mexico 8. Cucumber 1/4" Peeled Sliced Net Wt. 5 LB. Keep Refrigerated. Mexico
Lot/Code Info: Lot Codes: 1. X7544915, X7544941, X7545223, X7545254, X7545818, X7547379, X7549235, X7549567, X7552171. 2. X7544916, X7544942, X7545255, X7545671, X7545820, X7547380. 3. X7522892, X7525242, X7527841, X7529877, X7538875, X7544860, X7545305, X7546056, X7546374, X7548174, X7549360, X7550452, X7550665, X7550864, X7551649, X7552580, X7554639. 4. X7523208, X7525604, X7527034, X7527842, X7528437, X7530464, X7532041, X7532810, X7535312, X7536804, X7537516, X7543731, X7544783, X7545096, X7546437, X7546473, X7547169, X7547211, X7547672, X7548066, X7549528, X7550453, X7552059, X7552233, X7556439. 5. X7547984, X7548122, X7548232, X7549231, X7549555. 6. X7545151, X7549635, X7551987, X7556080, X7558549. Use By: 11/6/2024 - 11/13/2024. 7. X7568580, USE BY: 11/17/2024. 8. X7550999 and X7557325 USE BY: 11/8/2024 - 11/12/2024.
Quantity Affected: 1595 units
Reason for Recall
Cucumbers have potential to be contaminated with Salmonella.
Distribution
IA, IL, KS, MI, MN, MT, ND, NE, SD, WI, WY
Type: Voluntary: Firm initiated
Recall Initiated: 2024-12-01
Company
Saint Paul, MN
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 63 food recalls issued in the same week, part of 204 food-related FDA actions this month.
RUSS DAVIS WHOLESALE has 5 FDA actions in our database, including 5 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (RUSS DAVIS WHOLESALE) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does RUSS DAVIS WHOLESALE have FDA actions?
RUSS DAVIS WHOLESALE has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0367-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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