Skip to main content

Heinens Recall: Product contains undeclared pecans, a known allergen.

United States

TerminatedClass II

Company
Heinens
Product
Heinen's Tuscan Salad Bowl Ingredients: Garbanzo Beans***Dis…
Recall date
May 30, 2024
Terminated
June 21, 2024
Source
FDA

Reason for recall

Product contains undeclared pecans, a known allergen.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Heinen's Tuscan Salad Bowl Ingredients: Garbanzo Beans***Disodium EDTA***Arugula, Roasted Corn***Red Bell Pepper, Dried Cranberries***Walnuts***Parmesan Cheese*** Contains: WALNUT, MILK Not published in this source record 106 units MR252818

Distribution

  • Product was only distributed to Heinen retail locations in Illinois and Ohio.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1377-2024
Event ID
94751
Status
Terminated
Classification
Class II
Company
Heinens
Product description
Heinen's Tuscan Salad Bowl Ingredients: Garbanzo Beans***Disodium EDTA***Arugula, Roasted Corn***Red Bell Pepper, Dried Cranberries***Walnuts***Parmesan Cheese*** Contains: WALNUT, MILK
Quantity
106 units
Reason
Product contains undeclared pecans, a known allergen.
Recall initiation date
May 30, 2024
Report date
June 26, 2024
Classification date
Not published in this source record
Termination date
June 21, 2024
Distribution pattern
Product was only distributed to Heinen retail locations in Illinois and Ohio.
UPC, lot, and code information
MR252818
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Heinens

Other recalls from Heinens

FDA Recall United States Terminated Historical recordClass I

Heinens

Product
Heinen's Fresh Ground Cashew Butter: packaged in plastic cir…
Published
August 23, 2023
Distribution
Retail Locations in OH and IL

View recall →

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 II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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.