Recall record at a glance
| Official record | F-0190-2016 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Andrew & Williamson Fresh Produce |
| Report date | Nov 18, 2015 |
| Recall initiation date | Sep 4, 2015 |
| Quantity | 47,895 total units |
| Location | San Diego, CA, United States |
Official product description
1 1/9 Bushel Limited Edition Cucumber Carton, Sizes: Plains (60-84 count), Extra Large (48 count), Large (60 count), Super Select (72 count), Super Select Special (84 count). These cucumbers are shipped in a black, green, yellow, and craft colored carton which reads Limited Edition Pole Grown Cucumbers. This variety is often referred to as a Slicer or American cucumber. It has a dark green color. It typically has a length of 7 to 10 inches and a diameter of 1.75 to 2.5 inches.
Why the product was recalled
Andrew and Williamson Fresh Produce (A&W) is recalling all cucumbers sold under the Limited Edition label because it may be contaminated with Salmonella.
Distribution information
Limited Edition cucumbers were distributed in the states of Alaska, Arkansas, Arizona, California, Colorado, Florida, Idaho, Illinois, Kansas, Kentucky, Louisiana, Mississippi, Minnesota, Montana, New Jersey, New Mexico, Nevada, Oklahoma, Oregon, South Carolina, Texas, and Utah and reached customers through retail, food service companies, wholesalers, and brokers.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
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