Guayaki Brand Yerba Mate - Revel Berry; 16 oz aluminum can, Best By 12SEP16. UPC 6 32432 73777 5 Guayaki Yerba Mate is a high energy infusion made from the leaves of the celebrated South American mate tree. Guayaki S.R. P. Sebastopol, CA 95472 Certified Organic by CCOF Certified Fair Trade by IMO
Recalled by Guayaki S.r.p., INC. on Apr 17, 2015
Reason for Recall
Consumer complaints received of fermented, slimy, carbonated or moldy product in on lot of Guayaki Brand Yerba Mate Revel Berry.
Product Description
Guayaki Brand Yerba Mate - Revel Berry; 16 oz aluminum can, Best By 12SEP16. UPC 6 32432 73777 5 Guayaki Yerba Mate is a high energy infusion made from the leaves of the celebrated South American mate tree. Guayaki S.R. P. Sebastopol, CA 95472 Certified Organic by CCOF Certified Fair Trade by IMO
Distribution
US and one customer in Canada
What Should You Do?
- 1.Check your kitchen for this product immediately.
- 2.Do not consume the recalled product.
- 3.Return the product to where you bought it for a full refund, or throw it away.
- 4.If you have experienced any health issues, contact your healthcare provider.
Browse Related Recalls
Terms Explained
- Class II Recall — learn what this means in food safety
- FDA Food Recall — learn what this means in food safety
The this entity record above pulls directly from the FDA openFDA enforcement-report API. What follows is the per-entity context — how this entity sits in the broader U.S. FDA food, drug, and device recalls distribution and which underlying factors drive the headline numbers.
Every number on this page links back to the FDA openFDA enforcement-report API; the methodology page describes the inputs, refresh cadence, and known limitations of the underlying data product.
Practical use of this page is in combination with the comparison and ranking pages elsewhere on the site, which surface the same data for this entity’s peers within U.S. consumer-product recalls. A single-entity reading without peer context can be misleading when an entity is an outlier on one axis but typical on another.
Source: FDA Recalls, Market Withdrawals and Safety Alerts, 2026.