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Summer Fresh Salads Inc Recall: Product contains undeclared sesame.

United States

TerminatedClass I

Company
Summer Fresh Salads Inc
Product
Wegmans Harissa Hummus Topped With Harrisa 10.5 ounce (298 g…
Recall date
February 2, 2024
Terminated
March 4, 2025
Source
FDA

Reason for recall

Product contains undeclared sesame.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Wegmans Harissa Hummus Topped With Harrisa 10.5 ounce (298 g), clear plastic package with top, side and bottom labels. Not published in this source record Lot 240239: 268 cases; Lot 240309: 193 cases lot # 240239 and lot # 240309 with an expiration date of 03/19/2024 and 03/26/2024

Distribution

  • Washington D.C.
  • Delaware
  • Maryland
  • Massachusetts
  • New Jersey
  • New York
  • North Carolina
  • Pennsylvania
  • and Virginia

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1041-2024
Event ID
93931
Status
Terminated
Classification
Class I
Company
Summer Fresh Salads Inc
Product description
Wegmans Harissa Hummus Topped With Harrisa 10.5 ounce (298 g), clear plastic package with top, side and bottom labels.
Quantity
Lot 240239: 268 cases; Lot 240309: 193 cases
Reason
Product contains undeclared sesame.
Recall initiation date
February 2, 2024
Report date
March 13, 2024
Classification date
Not published in this source record
Termination date
March 4, 2025
Distribution pattern
Washington D.C., Delaware, Maryland, Massachusetts, New Jersey, New York, North Carolina, Pennsylvania, and Virginia
UPC, lot, and code information
lot # 240239 and lot # 240309 with an expiration date of 03/19/2024 and 03/26/2024
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Summer Fresh Salads Inc

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.