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SEVIROLI FOODSVERTULLO IMPORTS Recall: Product may contain foreign objects (metal).

United States

TerminatedClass II

Company
SEVIROLI FOODSVERTULLO IMPORTS
Product
HEB Jumbo Stuffed Shells; Jumbo Shells Filled with Creamy Ri…
Recall date
September 14, 2021
Terminated
August 26, 2022
Source
FDA

Reason for recall

Product may contain foreign objects (metal).

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
HEB Jumbo Stuffed Shells; Jumbo Shells Filled with Creamy Ricotta and Romano Cheese; NET WT. 22 OZ (1 LB 6OZ) 624g Not published in this source record 1349 cases Item Number 796702 Sell by 07/27/2022

Distribution

  • TX

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1021-2021
Event ID
88672
Status
Terminated
Classification
Class II
Company
SEVIROLI FOODSVERTULLO IMPORTS
Product description
HEB Jumbo Stuffed Shells; Jumbo Shells Filled with Creamy Ricotta and Romano Cheese; NET WT. 22 OZ (1 LB 6OZ) 624g
Quantity
1349 cases
Reason
Product may contain foreign objects (metal).
Recall initiation date
September 14, 2021
Report date
October 6, 2021
Classification date
Not published in this source record
Termination date
August 26, 2022
Distribution pattern
TX
UPC, lot, and code information
Item Number 796702 Sell by 07/27/2022
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: SEVIROLI FOODSVERTULLO IMPORTS

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Texas 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.