CLASS I Food recall · Reported 25 Mar 2026 · FDA Enforcement Report
Miss Vickies Spicy Dill Pickle recalled by Frito-lay North America
Frito-lay North America is recalling Miss Vickies Spicy Dill Pickle, distributed in Arkansas, Louisiana, Mississippi, New Mexico, Oklahoma, Texas. The recall was initiated on 3 Mar 2026 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0571-2026
- FDA event ID
- 98538
- Recalling firm
- Frito-lay North America, Plano, TX
- Brand
- Miss Vickies
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 3 Mar 2026
- FDA classified
- 17 Mar 2026
- Reported
- 25 Mar 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Undeclared Allergens
- Product category
- Fresh Herbs
Timeline
| 3 Mar 2026 | Recall initiated by company | |
| 17 Mar 2026 | Classified by FDA | +14 days |
| 25 Mar 2026 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared Allergen: Milk
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
Miss Vickies Spicy Dill Pickle; 8 oz bag
Where it was distributed
Arkansas, Louisiana, Mississippi, New Mexico, Oklahoma, and Texas.
Questions about this recall
Why was it recalled?
Undeclared Allergen: Milk
Which lots are affected?
"Guaranteed Fresh" date of 21 APR 2026 And one of these 9-digit Manufacturing Codes 38U301414 48U101514
Where was it sold?
Arkansas, Louisiana, Mississippi, New Mexico, Oklahoma, and Texas.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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