RecallRadar
High RiskReported March 25, 2026

Miss Vickies Spicy Dill Pickle

Recalled by FRITO-LAY NORTH AMERICA, INC.

Food recall

FRITO-LAY NORTH AMERICA, INC.

Class I — most serious

There is a reasonable chance that using this product could cause serious health problems or death.

See all recalls involving an undeclared allergen

FRITO-LAY NORTH AMERICA, INC. has recalled Miss Vickies Spicy Dill Pickle, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on March 25, 2026 and was initiated on March 3, 2026. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Miss Vickies Spicy Dill Pickle, with approximately 5,292 bags affected. The company behind the recall is FRITO-LAY NORTH AMERICA, INC., based in Plano, TX. The FDA describes the product as: “Miss Vickies Spicy Dill Pickle; 8 oz bag”

Why was Miss Vickies Spicy Dill Pickle recalled?

According to the FDA, the stated reason for the recall is: “Undeclared Allergen: Milk.” In plain terms, this recall relates to an undeclared ingredient or allergen.

An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.

What should you do?

If you think you may have bought Miss Vickies Spicy Dill Pickle, compare it against the product description and identifying codes ("Guaranteed Fresh" date of 21 APR 2026 And one of these 9-digit Manufacturing Codes 38U301414 48U101514) before using it.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact FRITO-LAY NORTH AMERICA, INC. or your local health authority.

About this recall

This recall was distributed in TX. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Terminated
Date reported
March 25, 2026
Recall started
March 3, 2026
Distributed in
TX
What was recalled
Miss Vickies Spicy Dill Pickle; 8 oz bag
Why it was recalled (as stated by the FDA)
Undeclared Allergen: Milk
How to identify the affected product
"Guaranteed Fresh" date of 21 APR 2026 And one of these 9-digit Manufacturing Codes 38U301414 48U101514
Amount recalled
5,292 bags

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was Miss Vickies Spicy Dill Pickle recalled?+

According to the FDA: Undeclared Allergen: Milk

How serious is this recall?+

Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.

What should I do if I have Miss Vickies Spicy Dill Pickle?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0571-2026. Information last synced from the FDA on July 6, 2026.