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
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
- Brand
- Blanched Penne
- 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 2021 | Recall initiated by company | |
| 11 May 2021 | Classified by FDA | +27 days |
| 19 May 2021 | Published 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.
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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