CLASS I Food recall · Reported 14 Mar 2018 · FDA Enforcement Report

Heinen's Potato Gnocchi * Preservative Free * recalled by La Pasta

La Pasta is recalling Heinen's Potato Gnocchi * Preservative Free *, distributed in Illinois, Ohio. The recall was initiated on 21 Feb 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLOT#1119-1120 / 1121-1122 / 1132-1133 / 2016-2017 / 2027-2028 / 2034-2035 / 2038-2039 / 2130-2131 / 2139-2140 / 2221-2222 / 2231-2232.
Quantity recalled208 cases

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-0909-2018
FDA event ID
79322
Recalling firm
La Pasta, Silver Spring, MD
Classification
Class I
Status
Terminated
Recall initiated
21 Feb 2018
FDA classified
8 Mar 2018
Reported
14 Mar 2018
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Milk
Product category
Potatoes

Timeline

21 Feb 2018Recall initiated by company
8 Mar 2018Classified by FDA+15 days
14 Mar 2018Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

LA PASTA, INC has initiated a recall of Heinen's Potato Gnocchi 9 oz. , because of a undeclared milk allergen .

Product as listed by the FDA

HEINEN'S Potato Gnocchi * Preservative Free * 9 oz. (225 g) in clear film plastic trays

Where it was distributed

The product was distributed to the following states IL and OH

IllinoisOhio

Questions about this recall

Why was it recalled?

LA PASTA, INC has initiated a recall of Heinen's Potato Gnocchi 9 oz. , because of a undeclared milk allergen .

Which lots are affected?

LOT#1119-1120 / 1121-1122 / 1132-1133 / 2016-2017 / 2027-2028 / 2034-2035 / 2038-2039 / 2130-2131 / 2139-2140 / 2221-2222 / 2231-2232.

Where was it sold?

The product was distributed to the following states IL and OH

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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