CLASS II Food recall · Reported 31 Jan 2018 · FDA Enforcement Report

Nestle Hot Pockets¿ Four Cheese Pizza Snack Bites recalled by Nestle U

Nestle USA is recalling Nestle Hot Pockets¿ Four Cheese Pizza Snack Bites, distributed in Missouri, Oklahoma. The recall was initiated on 8 Nov 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBatch Code 6327544616
Quantity recalled4200 lbs

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-0606-2018
FDA event ID
78542
Recalling firm
Nestle USA, Solon, OH
Brand
Nestle
Classification
Class II
Status
Terminated
Recall initiated
8 Nov 2017
FDA classified
23 Jan 2018
Reported
31 Jan 2018
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Undeclared Allergens
Product category
Frozen Pizza

Timeline

8 Nov 2017Recall initiated by company
23 Jan 2018Classified by FDA+76 days
31 Jan 2018Published 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

The firm distributed product without ingredient statement or labeling. Product contains various allergens.

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

Nestle HOT POCKETS¿ FOUR CHEESE PIZZA SNACK BITES in clear plastic bags.

Where it was distributed

Product was sent to the following states: MO & OK

MissouriOklahoma

Questions about this recall

Why was it recalled?

The firm distributed product without ingredient statement or labeling. Product contains various allergens.

Which lots are affected?

Batch Code 6327544616

Where was it sold?

Product was sent to the following states: MO & OK

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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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