4 oz. Complete Cookie, Chocolate Chip, UPC Code: 7 87692-83461 7, 12pks: 231,114 sleeves (contains 12 cookies) 6pks: 54,660 sleeves (c...
⚠ 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-1220-2017.
Lenny & Larrys is recalling Chocolate Chip and Coconut Chocolate Chip cookies due to the possible presence of undeclared milk in the dark chocolate chips.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1220-2017.
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 Lenny & Larry's, 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-1220-2017.
Lenny & Larry's, 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.
Lenny & Larry's, Inc. Recall FAQ
Lenny & Larry's, Inc. is the subject of a bakery & grains safety report: 4 oz. Complete Cookie, Chocolate Chip, UPC Code: 7 87692-83461 7, 12pks: 231,114 sleeves (contains 12 cookies) 6pks: 54,660 sleeves (c.... The notice was published on December 12, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 5,232,888 units are potentially affected.