CLASS III Food recall · Reported 21 Jan 2026 · FDA Enforcement Report

Publix Rice & Pigeon Peas recalled by ASK Foods

ASK Foods is recalling Publix Rice & Pigeon Peas, distributed in Florida. The recall was initiated on 16 Dec 2025 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codes5387-4, 5387-5, & 5387-6
Quantity recalled2078 units in total

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-0385-2026
FDA event ID
98190
Recalling firm
ASK Foods, Palmyra, PA
Brand
Publix
Classification
Class III
Status
Terminated
Recall initiated
16 Dec 2025
FDA classified
9 Jan 2026
Reported
21 Jan 2026
Type
Voluntary: Firm initiated
Customers notified by
Other
Reason category
Undeclared Allergens
Product category
Rice

Timeline

16 Dec 2025Recall initiated by company
9 Jan 2026Classified by FDA+24 days
21 Jan 2026Published in enforcement report+12 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 (Soy)

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

Publix Rice & Pigeon Peas, Net Wt 32 oz (2lb), Plastic tray with clear lid, black film, and a pre-printed label. 6 (2lb) containers per case .

Where it was distributed

The adulterated product was distributed to one state, FL

Florida

Stores named: Publix

Questions about this recall

Why was it recalled?

Undeclared Allergen (Soy)

Which lots are affected?

5387-4, 5387-5, & 5387-6

Where was it sold?

The adulterated product was distributed to one state, FL

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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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