Wavy Lay s Original Potato Chips UPC 0 28400 04380 9 packaged in flexible bag
Summary
The FDA issued a Class I for Wavy Lay s Original Potato Chips UPC 0 28400 04380 9 packaged in flexible bag by Frito-Lay, Inc. Headquarters. Reason: May contain undeclared milk.
Details
Source
Food Recall
External ID
F-0885-2021
Action Date
2021-09-01
Status
Terminated
Category
food
Product Description
Wavy Lay s Original Potato Chips UPC 0 28400 04380 9 packaged in flexible bag
Lot/Code Info: Either (1) or (2) (1) Must have both Guaranteed Fresh date of 02 Nov 2021 And the Manufacturing Code 1712 17944 85 21:30 (2) Must have both Guaranteed Fresh date of 19 Oct 2021 And the Manufacturing Code 1713 20044 18 03:37
Quantity Affected: 36 bags
Reason for Recall
May contain undeclared milk
Distribution
North Carolina, South Carolina and Virginia
Type: Voluntary: Firm initiated
Recall Initiated: 2021-08-11
Company
Plano, TX
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 40 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frito-Lay, Inc. Headquarters has 8 FDA actions in our database, including 8 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Frito-Lay, Inc. Headquarters) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Frito-Lay, Inc. Headquarters have FDA actions?
Frito-Lay, Inc. Headquarters has 8 FDA actions in our database, including 8 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0885-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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