SunRidge Organic Crunchy Peanut Butter with salt Packed in 35 pound tub UPC code: 086700161852 Manufactured by Falcon Trading Company...
⚠ 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-0325-2013.
Falcon Trading Company Inc. used peanut butter in their products that is now under recall by Sunland Inc. due to potential Salmonella contamination.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0325-2013.
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 Falcon Trading 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-0325-2013.
Falcon Trading 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.
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.
Falcon Trading Co., Inc. Recall FAQ
Falcon Trading Co., Inc. is the subject of a dairy safety report: SunRidge Organic Crunchy Peanut Butter with salt Packed in 35 pound tub UPC code: 086700161852 Manufactured by Falcon Trading Company.... The notice was published on September 25, 2012 by the U.S. Food and Drug Administration (FDA). Approximately 0 units are potentially affected.