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CriticalFDAfda-F-1854-2018UNDECLARED ALLERGEN

Oatmeal Raisin Cookies, brand Cafe YUMM! Product is packaged in shrink wrapped master case. Each master case contains two boxes and eac...

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Units Affected
48
Recall Date
August 15, 2018
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1854-2018.

Oatmeal Raisin Cookies are recalled because cookies may contain undeclared peanuts.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1854-2018.

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 Marsee Foods Inc 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-1854-2018.

Marsee Foods Inc

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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Marsee Foods Inc Recall FAQ

Marsee Foods Inc is the subject of a bakery & grains safety report: Oatmeal Raisin Cookies, brand Cafe YUMM! Product is packaged in shrink wrapped master case. Each master case contains two boxes and eac.... The notice was published on August 15, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 48 units are potentially affected.