Skip to main content
High RiskFDAfda-F-1495-2019UNDECLARED ALLERGEN

White Chocolate Raspberry Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117

Category
Units Affected
207
Recall Date
May 31, 2019
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1495-2019.

Packaged cheesecakes are distributed with no labels indicating the ingredients or the major food allergens they contain.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1495-2019.

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 Hank's Cheesecakes, 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-1495-2019.

Hank's Cheesecakes, LLC

FDA

About the U.S. Food and Drug Administration

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

Visit FDA.gov →

📣 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.

How to report to FDAFile a report at FDA

Hank's Cheesecakes, Llc Recall FAQ

Hank's Cheesecakes, Llc is the subject of a dairy safety report: White Chocolate Raspberry Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117. The notice was published on May 31, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 207 units are potentially affected.