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Frito-Lay, Inc. Headquarters Recall: Potential to contain undeclared milk

United States

TerminatedClass I

Company
Frito-Lay, Inc. Headquarters
Product
Ruffles All Dressed Potato Chips 16 1/8 oz. packaged in flex…
Recall date
May 4, 2021
Terminated
July 9, 2021
Source
FDA

Reason for recall

Potential to contain undeclared milk

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Ruffles All Dressed Potato Chips 16 1/8 oz. packaged in flexible plastic bags UPC 28400 56520 Not published in this source record 5232 bags Both Guaranteed Fresh date of 1 JUN 2021 And one of these 9-digit Manufacturing Codes 373205510 473305610 473105610

Distribution

  • Alabama
  • Florida
  • Georgia
  • Louisiana
  • Mississippi
  • North Carolina
  • South Carolina
  • Tennessee
  • and Virginia.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0660-2021
Event ID
87878
Status
Terminated
Classification
Class I
Company
Frito-Lay, Inc. Headquarters
Product description
Ruffles All Dressed Potato Chips 16 1/8 oz. packaged in flexible plastic bags UPC 28400 56520
Quantity
5232 bags
Reason
Potential to contain undeclared milk
Recall initiation date
May 4, 2021
Report date
June 16, 2021
Classification date
Not published in this source record
Termination date
July 9, 2021
Distribution pattern
Alabama, Florida, Georgia, Louisiana, Mississippi, North Carolina, South Carolina, Tennessee, and Virginia.
UPC, lot, and code information
Both Guaranteed Fresh date of 1 JUN 2021 And one of these 9-digit Manufacturing Codes 373205510 473305610 473105610
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Letter
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Frito-Lay, Inc. Headquarters

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Product
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Distribution
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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.