Sliced Cucumber (Triple B Corporation) – Salmonella risk (2015)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Cucumber, sliced 3/8", product is packaged in a 2 lbs. plastic bag and placed in a cardboard box. Product is sold to deli department at retail store and it is not sold directly to consumers. The UPC is 0 45009 10104 4.
Brand
Triple B Corporation
Lot Codes / Batch Numbers
GTIN# 1 0045009 10104 1, Use By dates include 8/8/15 and up to 9/11/15.
Products Sold
GTIN# 1 0045009 10104 1, Use By dates include 8/8/15 and up to 9/11/15.
Triple B Corporation is recalling Cucumber, sliced 3/8", product is packaged in a 2 lbs. plastic bag and placed in a cardboard box. due to Cucumber, sliced 3/8", is recalled due to a potential contamination with Salmonella. Sliced cucumber is linked to the current recall of Limited Editi. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Cucumber, sliced 3/8", is recalled due to a potential contamination with Salmonella. Sliced cucumber is linked to the current recall of Limited Edition Brand Cucumbers being conducted by Andrew & Williamson Fresh Produce.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AK, IN
Page updated: Jan 6, 2026