Ingomar Packing Co Recall: Foreign object; plastic

🇺🇸 United States

1. August 3, 2023 - Recall initiated
2. January 17, 2024 - Reported by source
3. August 1, 2024 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0709-2024

Event ID

93608

Status

Terminated

Classification

Class II

Company

Ingomar Packing Co

Product description

3/4" Diced Tomatoes in Juice packed in 55 gallon metal drums

Quantity

178 drums

Reason

Foreign object; plastic

Recall initiation date

August 3, 2023

Report date

January 17, 2024

Classification date

Not published in this source record

Termination date

August 1, 2024

Distribution pattern

U.S. Distribution to CA and WA. Foreign distribution to Japan.

UPC, lot, and code information

Product code 9777135DF/Lot codes: V01007292022 V14807292022 V02307292022 V18607292022 V18807292022 V14907292022 V02407292022 V18707292022 V16407292022 V15407292022 V02507292022 V01507292022 V01207292022 V15507292022 V02607292022 V01107292022 V01307292022 V15607292022 V03207292022 V00807292022 V05907292022 V15807292022 V03307292022 V00907292022 V03707292022 V12907292022 V03407292022 V07907292022 V08707292022 V13007292022 V03507292022 V08007292022 V02707292022 V13107292022 V04007292022 V08107292022 V02807292022 V13207292022 V04107292022 V07407292022 V02907292022 V13707292022 V04207292022 V07507292022 V03007292022 V13807292022 V04307292022 V07607292022 V03107292022 V13907292022 V04807292022 V07707292022 V17807292022 V16507292022 V04907292022 V14107292022 V17907292022 V17407292022 V05007292022 V14207292022 V18007292022 V17507292022 V05107292022 V14307292022 V18107292022 V10707292022 V05207292022 V14407292022 V03607292022 V10807292022 V05707292022 V15007292022 V03807292022 V10907292022 V11507292022 V15107292022 V08607292022 V11007292022 V11607292022 V15207292022 V00207292022 V16307292022 V11707292022 V15307292022 V00307292022 V09007292022 V11807292022 V15907292022 V00407292022 V09107292022 V12407292022 V13407292022 V00507292022 V09207292022 V12507292022 V13507292022 V00607292022 V09307292022 V05807292022 V13607292022 V01907292022 V09807292022 V06007292022 V17607292022 V02007292022 V09907292022 V06507292022 V17707292022 V02107292022 V10007292022 V06607292022 V16007292022 V02207292022 V10107292022 V06707292022 V16107292022 V10607292022 V10207292022 V06807292022 V16207292022 V11107292022 V03907292022 V07807292022 V11207292022 V04407292022 V12607292022 V11307292022 V04507292022 V12807292022 V11407292022 V04607292022 V13307292022 V11907292022 V04707292022 V00107292022 V12007292022 V05307292022 V00707292022 V12107292022 V05407292022 V01607292022 V12207292022 V05507292022 V01707292022 V12307292022 V05607292022 V01807292022 V08807292022 V06107292022 V16707292022 V08907292022 V06207292022 V16807292022 V09407292022 V06307292022 V16907292022 V09507292022 V06407292022 V17007292022 V09607292022 V06907292022 V17107292022 V09707292022 V07007292022 V18407292022 V10307292022 V07107292022 V18507292022 V10407292022 V07207292022 V16607292022 V10507292022 V07307292022 V17207292022 V14007292022 V08207292022 V17307292022 V14507292022 V08307292022 V18207292022 V14607292022 V08407292022 V18307292022 V14707292022 V08507292022 V01407292022

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

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 93608 with 1 other product entry in Public Health Trace.

Responsible company: Ingomar Packing Co

Other recalls from Ingomar Packing Co

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

Distributed No data published

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
California	1
Washington	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: July 18, 2026 ET

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.

• Email
• X / Twitter
• Facebook