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Le Chef Bakery Recall: undeclared colors (yellow#5)

United States

OngoingClass II

Company
Le Chef Bakery
Product
Le Chef Bakery branded Mini Italian Pastry Assortment; 2.5 l…
Recall date
June 10, 2026
Source
FDA

Reason for recall

undeclared colors (yellow#5)

  1. - Recall initiated
  2. - Reported by source
Recalled products
Product description UPC Quantity Lot / code information
Le Chef Bakery branded Mini Italian Pastry Assortment; 2.5 lbs/cs; (40 pieces/cs); packaged in generic food service packaging with white label. UPC: MP006 Not published in this source record 2595 units Julian Dates 3355 to 1536 (mfg. dates: 12/01/2025 to 06/02/2026)

Distribution

  • Recalled products are intended for commercial and institution use. Examples are hotels
  • universities
  • and buisnesses in the south-west states of California
  • Arizona and Nevada.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
N/A
Event ID
99205
Status
Ongoing
Classification
Class II
Company
Le Chef Bakery
Product description
Le Chef Bakery branded Mini Italian Pastry Assortment; 2.5 lbs/cs; (40 pieces/cs); packaged in generic food service packaging with white label. UPC: MP006
Quantity
2595 units
Reason
undeclared colors (yellow#5)
Recall initiation date
June 10, 2026
Report date
July 8, 2026
Classification date
Not published in this source record
Termination date
Not terminated as of this source record
Distribution pattern
Recalled products are intended for commercial and institution use. Examples are hotels, universities, and buisnesses in the south-west states of California, Arizona and Nevada.
UPC, lot, and code information
Julian Dates 3355 to 1536 (mfg. dates: 12/01/2025 to 06/02/2026)
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: Le Chef Bakery

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 "Ongoing." 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.