New Seasons Market Creamy Almond Butter 16oz; Label reads in part "***NEW SEASONS WILD FRIENDS FOODS PORTLAND, OR *** IT'S A JAR OF ALM...
⚠ 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-0209-2017.
New Seasons Markets is recalling their brand name Almond Butter due to a labeling error. Some of the jars labeled Almond Butter actually contain Peanut Butter.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0209-2017.
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 New Seasons Market 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-0209-2017.
NEW SEASONS MARKET
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.
New Seasons Market Recall FAQ
New Seasons Market is the subject of a dairy safety report: New Seasons Market Creamy Almond Butter 16oz; Label reads in part "***NEW SEASONS WILD FRIENDS FOODS PORTLAND, OR *** IT'S A JAR OF ALM.... The notice was published on September 12, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 3,741 units are potentially affected.