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Bob Evans Farms (BEF) Recall: Potential for foreign material - Red Plastic

United States

TerminatedClass II

Company
Bob Evans Farms (BEF)
Product
Bob Evan's Original Mash Potato 2lbs (32 oz) packaged in bla…
Recall date
March 4, 2024
Terminated
April 4, 2024
Source
FDA

Reason for recall

Potential for foreign material - Red Plastic

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Bob Evan's Original Mash Potato 2lbs (32 oz) packaged in black plastic tray with clear film and corrugate sleeve overwrap. 6 units per case Not published in this source record 410 cases Batch No. 2392939 Lot No KCL1 4-18-2024 Product No 10000534 UPC 75900005349 Packer No KCL1 Best By 4/18/24

Distribution

  • Connecticut
  • Illinois
  • Massachusetts
  • New York
  • Ohio
  • Pennsylvania
  • Vermont
  • Wisconsin

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1085-2024
Event ID
94177
Status
Terminated
Classification
Class II
Company
Bob Evans Farms (BEF)
Product description
Bob Evan's Original Mash Potato 2lbs (32 oz) packaged in black plastic tray with clear film and corrugate sleeve overwrap. 6 units per case
Quantity
410 cases
Reason
Potential for foreign material - Red Plastic
Recall initiation date
March 4, 2024
Report date
March 27, 2024
Classification date
Not published in this source record
Termination date
April 4, 2024
Distribution pattern
Connecticut, Illinois, Massachusetts, New York, Ohio, Pennsylvania, Vermont, Wisconsin
UPC, lot, and code information
Batch No. 2392939 Lot No KCL1 4-18-2024 Product No 10000534 UPC 75900005349 Packer No KCL1 Best By 4/18/24
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: Bob Evans Farms (BEF)

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.