Sunshine Bakery Recall: The products are being recalled because the labeling does not declare food allergens peanuts, coconuts, almonds and cashews on the label..

🇺🇸 United States

1. March 24, 2017 - Recall initiated
2. April 26, 2017 - Reported by source
3. May 31, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-2083-2017

Event ID

76860

Status

Terminated

Classification

Class I

Company

Sunshine Bakery

Product description

Cassava Cake (Khoa Mi) in strips or cake form, individually packaged in clear wrap and Styrofoam tray, with a printed label on top. Best by date is printed on the label. 5 oz/141 grams per unit with UPC code 015200401304

Quantity

320 units

Reason

The products are being recalled because the labeling does not declare food allergens peanuts, coconuts, almonds and cashews on the label..

Recall initiation date

March 24, 2017

Report date

April 26, 2017

Classification date

Not published in this source record

Termination date

May 31, 2017

Distribution pattern

Products were distributed to retail stores in California, Texas and Nevada.

UPC, lot, and code information

All products with best by dates of 03/24 and older. Products were sold to retail stores in 2/24/2017

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Press Release

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 76860 with 1 other product entry in Public Health Trace.

Responsible company: Sunshine Bakery

Other recalls from Sunshine 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: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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