CLASS I Food recall · Reported 13 May 2015 · FDA Enforcement Report

Blintzes with Potato & Mushroom, Net recalled by Royal Frozen Food

Royal Frozen Food is recalling Blintzes with Potato & Mushroom, Net, distributed in California, Nevada. The recall was initiated on 20 Apr 2015 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUPC 6 0723830020 1
Quantity recalled3,600 units 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
F-2149-2015
FDA event ID
71030
Recalling firm
Royal Frozen Food, Los Angeles, CA
Classification
Class I
Status
Terminated
Recall initiated
20 Apr 2015
FDA classified
1 May 2015
Reported
13 May 2015
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Undeclared Milk
Product category
Fish

Timeline

20 Apr 2015Recall initiated by company
1 May 2015Classified by FDA+11 days
13 May 2015Published 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

Royal Frozen Food is recalling Royal Frozen Food Blintzes because they contain undeclared milk.

Product as listed by the FDA

Blintzes with Potato & Mushroom, Net. Wt. 18oz (510g), 10 pieces. 18-oz. plastic trays containing ten pieces of Royal Frozen Food, BLINTZES Blintzes with Potato Mushroom with bar code 6 0723830020 1. 12 packs per case.

Where it was distributed

CA & NV

CaliforniaNevada

Questions about this recall

Why was it recalled?

Royal Frozen Food is recalling Royal Frozen Food Blintzes because they contain undeclared milk.

Which lots are affected?

UPC 6 0723830020 1

Where was it sold?

CA & NV

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.

Other products in this recall event

2 other products · FDA event 71030

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