Schmidt Baking Co., Inc. Recall: Schmidt Baking Company has decided to initiate a recall of various bread products, after being informed by one of their vendors that the ingredient supplied to them by the vendor is under recall. Potential of foreign material in product.

🇺🇸 United States

1. December 27, 2017 - Recall initiated
2. March 7, 2018 - Reported by source
3. March 1, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0841-2018

Event ID

78837

Status

Terminated

Classification

Class II

Company

Schmidt Baking Co., Inc.

Product description

BNS WHEAT ROLLS ( Under the following Trade Names - Giant, Harvest Pride, Shoppers and Old Tyme )

Quantity

1356 Tray Count

Reason

Schmidt Baking Company has decided to initiate a recall of various bread products, after being informed by one of their vendors that the ingredient supplied to them by the vendor is under recall. Potential of foreign material in product.

Recall initiation date

December 27, 2017

Report date

March 7, 2018

Classification date

Not published in this source record

Termination date

March 1, 2018

Distribution pattern

Product was distributed to various retail distribution centers in the United States Maryland, Delaware, Virginia, West Virginia, Connecticut, Pennsylvania, New Jersey, New York.

UPC, lot, and code information

Julian code Dates are - 344, and 345

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

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 78837 with 10 other product entries in Public Health Trace.

Responsible company: Schmidt Baking Co., Inc.

Other recalls from Schmidt Baking Co., 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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