Lemon Dessert Bars packaged under Schwartz Brothers Bakery brand in a 11.6 oz (328g), kraft packaging with UPC 7 17887 65163 7. The la...
⚠ 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.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0127-2020.
Lemon Dessert Bars product is recalled due to undeclared egg.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0127-2020.
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 Schwartz Brothers Restaurants Dba Schwartz Brothers Bakery 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-0127-2020.
Schwartz Brothers Restaurants dba Schwartz Brothers Bakery
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.
Schwartz Brothers Restaurants Dba Schwartz Brothers Bakery Recall FAQ
Schwartz Brothers Restaurants Dba Schwartz Brothers Bakery is the subject of a dairy safety report: Lemon Dessert Bars packaged under Schwartz Brothers Bakery brand in a 11.6 oz (328g), kraft packaging with UPC 7 17887 65163 7. The la.... The notice was published on September 16, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 24 units are potentially affected.