FRONT: Stauffer's Animal Crackers Original; Net Wt. 32 OZ.; BACK: (best by date): 07SEP17; (bag lot numbers) LC120716 or LD120716; ...
⚠ 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-1343-2017.
D. F. Stauffer Biscuit Co., Inc. is voluntarily recalling one specific best by date of 32 oz. Original Animal Crackers because they may be packaged with other cookies that contain milk powder.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1343-2017.
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 D. F. Stauffer Biscuit Co, 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-1343-2017.
D. F. Stauffer Biscuit Co, 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.
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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.
D. F. Stauffer Biscuit Co, Inc. Recall FAQ
D. F. Stauffer Biscuit Co, Inc. is the subject of a bakery & grains safety report: FRONT: Stauffer's Animal Crackers Original; Net Wt. 32 OZ.; BACK: (best by date): 07SEP17; (bag lot numbers) LC120716 or LD120716; .... The notice was published on January 18, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 2,268 units are potentially affected.