RECALL RECORD — CLASS IRecall closedF-0902-2013/FDA enforcement
Sugar Flowers Plus·Food·Dec 7, 2012

Pastillage (Gum Paste) Flowers

What you need to know

Class I
  • What happened

    Sugar Flowers Plus Inc of Glendale, CA is recalling Cake Decors Pastillage (gum paste) Flowers because of the undeclared use of egg white wash as a glue for the inner petals of…

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall closed · classified by the FDANationwide (US)More food

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Product identification

Source: FDA FOOD

Brand nameSugar Flowers Plus
Recalling firmSugar Flowers PlusGlendale, CA, United States
UPC / barcodes
8 38437 00004 7
Lot / date codes
  • Rose - Blue UPC code: 8 38437 00004 7
Distribution area
Nationwide

Nationwide.

United States

Quantity affectedNot provided by the FDA.
Recall initiationFDA report date: January 23, 2013
FDA recall numberF-0902-2013

Beyond the headline

The recall, in context

Sugar Flowers Plus initiated this food recall on December 7, 2012. The FDA enforcement report states: Sugar Flowers Plus Inc of Glendale, CA is recalling Cake Decors Pastillage (gum paste) Flowers because of the undeclared use of egg white wash as a glue for the inner petals of flowers. The FDA report lists distribution as: Nationwide.

The FDA enforcement report describes the reason as: Sugar Flowers Plus Inc of Glendale, CA is recalling Cake Decors Pastillage (gum paste) Flowers because of the undeclared use of egg white wash as a glue for the inner petals of flowers.

Pastillage (Gum Paste) Flowers was made or distributed by Sugar Flowers Plus in Glendale, CA, United States. This page reflects FDA report F-0902-2013, dated January 23, 2013.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared egg

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with an egg allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed egg allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have an egg allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Pastillage (Gum Paste) Flowers recall?

Sugar Flowers Plus recalled Pastillage (Gum Paste) Flowers in an FDA Class I enforcement action reported as F-0902-2013. Sugar Flowers Plus Inc of Glendale, CA is recalling Cake Decors Pastillage (gum paste) Flowers because of the undeclared use of egg white wash as a glue for the inner petals of…

What are the symptoms of Undeclared egg exposure?

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with an egg allergy.

How quickly can Undeclared egg symptoms appear?

Reactions can begin within minutes to a few hours after eating the product.

Who is most at risk from Undeclared egg?

People with a diagnosed egg allergy, especially children and anyone with a history of anaphylaxis.

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have an egg allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

How do I get a refund from Sugar Flowers Plus?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-0902-2013 and keep the packaging, lot code and proof of purchase if you have them.

Is the Sugar Flowers Plus recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0902-2013. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.