FDA recall record

Sam Dry Fruits and Enterprises Inshell R/S 21/25 US- Select Pistachios recall — FDA F-0617-2019

Positive result for Salmonella received while investigating to determine supplier of direct customer's positive findings also for Salmonella

Class Iclassification
F-0617-2019official record ID
Nov 14, 2018report date

Recall record at a glance

Official recordF-0617-2019
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmSam Dry Fruits and Enterprises Inc.
Report dateNov 14, 2018
Recall initiation dateOct 23, 2018
Quantity18, 225 lbs.
LocationModesto, CA, United States

Official product description

Inshell R/S 21/25 US- Select Pistachios; NET WT. 25 lb. (11.34kg) Product of the USA Production Date: 8/2018 ARO Pistachios Inc. 19750 Avenue 88, Terra Bella, CA 93270

Why the product was recalled

Positive result for Salmonella received while investigating to determine supplier of direct customer's positive findings also for Salmonella

Distribution information

NJ, MD, NY, PA, NJ

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: E-Mail.

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.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.