Pride of Iowa Sandwiches, Inc. Recall: The firm received a recall notice for an ingredient, ready-to-eat beef patties, which were potentially contaminated with foreign metal material. The patties were used in the manufacture of sandwiches.

🇺🇸 United States

1. October 29, 2019 - Recall initiated
2. November 13, 2019 - Reported by source
3. November 18, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0133-2020

Event ID

84162

Status

Terminated

Classification

Class II

Company

Pride of Iowa Sandwiches, Inc.

Product description

J. BOS Vending Service Monster Cheeseburger, Net Wt. 7.3 oz individually wrapped in plastic, packaged 24 count per case.

Quantity

8 cases/192 units

Reason

The firm received a recall notice for an ingredient, ready-to-eat beef patties, which were potentially contaminated with foreign metal material. The patties were used in the manufacture of sandwiches.

Recall initiation date

October 29, 2019

Report date

November 13, 2019

Classification date

Not published in this source record

Termination date

November 18, 2019

Distribution pattern

Distributed to food vending distributors in Michigan and Texas

UPC, lot, and code information

Production dates between 040919 and 281019.

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

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 84162 with 3 other product entries in Public Health Trace.

Responsible company: Pride of Iowa Sandwiches, Inc.

Other recalls from Pride of Iowa Sandwiches, Inc.

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.

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