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Bread Alone, Inc. Recall: Product contains undeclared sulfites.

United States

TerminatedClass II

Company
Bread Alone, Inc.
Product
Bread Alone Fruit & Nut Sourdough; packaged in 27 ounce plas…
Recall date
March 23, 2022
Terminated
December 8, 2023
Source
FDA

Reason for recall

Product contains undeclared sulfites.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Bread Alone Fruit & Nut Sourdough; packaged in 27 ounce plastic bag Not published in this source record 838 loaves Effected Codes: all product Fruit and Nut Sourdough in expiry with expiration dates before and including 3/28/22 Manufacturing date range: 3/15/22-3/22/22 UPC: 0 40345 00290 1

Distribution

  • NY
  • MA
  • CT

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0966-2022
Event ID
89884
Status
Terminated
Classification
Class II
Company
Bread Alone, Inc.
Product description
Bread Alone Fruit & Nut Sourdough; packaged in 27 ounce plastic bag
Quantity
838 loaves
Reason
Product contains undeclared sulfites.
Recall initiation date
March 23, 2022
Report date
April 13, 2022
Classification date
Not published in this source record
Termination date
December 8, 2023
Distribution pattern
NY, MA, CT
UPC, lot, and code information
Effected Codes: all product Fruit and Nut Sourdough in expiry with expiration dates before and including 3/28/22 Manufacturing date range: 3/15/22-3/22/22 UPC: 0 40345 00290 1
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

Responsible company: Bread Alone, Inc.

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
New York 1
Massachusetts 1
Connecticut 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.