Picnic Gourmet Spreads ( Tandoori Garlic Cheese Spread) 8 oz containers .12 Containers per case
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (listeria). 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-0728-2016.
Maryland Department of Health and Mental Hygiene (DHMH) collected a sample collected a sample of Red Pepper Feta Cheese Spread that came up positive for L. Monocytogenes. The analysis was done by the DHMH Laboratories Administration and revealed the presence of Listeria Monocytogenes in the product. The product is made by Picnic Gourmet Spreads, Potomac , MD 20854
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0728-2016.
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 Picnic Gourmet Spreads 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-0728-2016.
Picnic Gourmet Spreads 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.
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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.
Picnic Gourmet Spreads Llc Recall FAQ
Picnic Gourmet Spreads Llc is the subject of a dairy safety report: Picnic Gourmet Spreads ( Tandoori Garlic Cheese Spread) 8 oz containers .12 Containers per case. The notice was published on September 17, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 0 units are potentially affected.