CLASS I Food recall · Reported 19 May 2021 · FDA Enforcement Report

Blanched Penne Rigati recalled by T Marzetti Innovation Center

T Marzetti Innovation Center is recalling Blanched Penne Rigati, distributed in California. The recall was initiated on 14 Apr 2021 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesCase Code 10219CPC Product Bag Codes 10219C1PC & 10219C2PC
Quantity recalled210 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-0487-2021
FDA event ID
87736
Recalling firm
T Marzetti Innovation Center, Lewis Center, OH
Classification
Class I
Status
Terminated
Recall initiated
14 Apr 2021
FDA classified
11 May 2021
Reported
19 May 2021
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Egg
Product category
Other

Timeline

14 Apr 2021Recall initiated by company
11 May 2021Classified by FDA+27 days
19 May 2021Published 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 Egg Allergen

Product as listed by the FDA

Blanched Penne Rigati 8oz plastic bag 40 bags per case

Where it was distributed

Product was sent to a single consignee located in San Bernardino, CA. The consignee is a relabler/repacker who create Home Chief Meal Kits.

California

Questions about this recall

Why was it recalled?

Undeclared Egg Allergen

Which lots are affected?

Case Code 10219CPC Product Bag Codes 10219C1PC & 10219C2PC

Where was it sold?

Product was sent to a single consignee located in San Bernardino, CA. The consignee is a relabler/repacker who create Home Chief Meal Kits.

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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