Late July Organic Mini Peanut Butter Sandwich Crackers packaged in : 5oz box UPC 890444000700 8ct carton/1.125oz (single serve caddy...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (Salmonella contamination). 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-0291-2013.
Organic Mini Peanut Butter Sandwich Crackers are recalled due to Sunland peanut butter recall due to the potential to be contaminated with Salmonella
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0291-2013.
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 Late July Snacks, Llc 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-0291-2013.
Late July Snacks, LLC
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.
Late July Snacks, Llc Recall FAQ
Late July Snacks, Llc is the subject of a dairy safety report: Late July Organic Mini Peanut Butter Sandwich Crackers packaged in : 5oz box UPC 890444000700 8ct carton/1.125oz (single serve caddy.... The notice was published on September 28, 2012 by the U.S. Food and Drug Administration (FDA). Approximately 12,681 units are potentially affected.