Check the Batch
Class ITerminated in FDA datasetRecall initiated Jul 15, 2019

PitaPal Roasted Red Pepper Hummus 10 oz.

Recalling firm: Pita Pal Foods LP

Why it was recalled

Product has potential to be contaminated with Listeria monocytogenes

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Apr 13, 2020.

Check your package

Compare the exact product and package details with the label you have.

ProductPitaPal Roasted Red Pepper Hummus 10 oz. UPC 850157000664 and 32 oz. UPC 85157000344 7 and 5 lbs UPC 850157000237 packaged in plastic tub with clear lid with green rim. and white plastic tub with white lid.
Package size10 oz
UPC850157000237, 850157000664, 851570003447

FDA code information

Use By: 07/25/19 thru 09/18/19

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

PitaPal Roasted Red Pepper Hummus 10 oz. UPC 850157000664 and 32 oz. UPC 85157000344 7 and 5 lbs UPC 850157000237 packaged in plastic tub with clear lid with green rim. and white plastic tub with white lid.

Extracted codes and context

TypeCode / valueContext
UPC850157000237epper Hummus 10 oz. UPC 850157000664 and 32 oz. UPC 85157000344 7 and 5 lbs UPC 850157000237 packaged in plastic tub with clear lid with green rim. and white plastic tub with white lid.
UPC850157000664PitaPal Roasted Red Pepper Hummus 10 oz. UPC 850157000664 and 32 oz. UPC 85157000344 7 and 5 lbs UPC 850157000237 packaged in plastic tub with clear lid with green rim. and whit
UPC851570003447PitaPal Roasted Red Pepper Hummus 10 oz. UPC 850157000664 and 32 oz. UPC 85157000344 7 and 5 lbs UPC 850157000237 packaged in plastic tub with clear lid with green rim. and white plastic tub with white lid.

Original FDA recall reason

Product has potential to be contaminated with Listeria monocytogenes

Recall details

Recall number
F-2187-2019
Event ID
83343
FDA status
Terminated
Initiated
Jul 15, 2019
Reported
Sep 25, 2019
Classified
Sep 16, 2019
Terminated
Apr 13, 2020
Quantity
2816 cases
Location
Houston, TX, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Nationwide throughout the US

FDA source record · F-2187-2019

Data updated September 16, 2026. View official FDA data ↗

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