All varieties and packaging configurations of iced cut out cookies, labeled as Decorated Cut Out Cookie and Cut Out Cookies, 1oz and 2oz ...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (laceration). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2043-2015.
Cut Out Cookies sold in Giant Eagle Bakeries were recalled due to an undeclared milk allergen detected after receiving a consumer complaint of an allergic reaction.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2043-2015.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Giant Eagle, Inc. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- 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-2043-2015.
Giant Eagle, Inc.
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.
Giant Eagle, Inc. Recall FAQ
Giant Eagle, Inc. is the subject of a bakery & grains safety report: All varieties and packaging configurations of iced cut out cookies, labeled as Decorated Cut Out Cookie and Cut Out Cookies, 1oz and 2oz .... The notice was published on March 17, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 0 units are potentially affected.