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High RiskFDAfda-F-1223-2017CONTAMINATION

ALN UNICED 1/4 Sheet Split Layer White Cake, Item 00886, three stacked cake layers with plastic liner in between layers are packaged in a...

Units Affected
3,314
Recall Date
December 19, 2016
Issuing Agency
Hazard
Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1223-2017.

ALN UNICED ¿ Sheet Split Layer White Cake, a box of 12 cakes, is recalled due to a potential contamination with walnut and label does not declare walnut.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1223-2017.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Portland Specialty Baking Llc or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1223-2017.

Portland Specialty Baking LLC

FDA

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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Portland Specialty Baking Llc Recall FAQ

Portland Specialty Baking Llc is the subject of a bakery & grains safety report: ALN UNICED 1/4 Sheet Split Layer White Cake, Item 00886, three stacked cake layers with plastic liner in between layers are packaged in a.... The notice was published on December 19, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 3,314 units are potentially affected.