FDA recall, , Moderate risk
Frederik's by Meijer Vanilla Bourbon Trail Mix
Frederik's by Meijer Vanilla Bourbon Trail Mix may contain undeclared wheat and soy, posing a risk of serious allergic reaction.
Recall ended Jul 14, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
Ferris Coffee and Nut Company, Inc., of Grand Rapids, Michigan, recalled a single lot of Frederik's by Meijer Vanilla Bourbon Trail Mix, packed in plastic retail-sized black bags NET WT 9 OZ (255g), because it may contain undeclared wheat and soy. People who have an allergy or severe sensitivity to wheat or soy run the risk of serious or life-threatening allergic re. The company began the recall on April 21, 2026, and announced it on April 23, 2026.
2 photos
What to do
If a code on your package is listed below:
- Consumers who have purchased 9 ounce packages of Frederik’s by Meijer Vanilla Bourbon Trail Mix with lot # 6069-1 on the back and an expiration date of 12/10/26 are urged to throw them away or return them to the place of purchase for a full refund.
- Consumers with questions may contact the company at 1-877-363-4537 7:00 AM – 10 PM EDT.
Is your mix affected?
Match the list below, then check the codes the FDA notice also names.
A UPC is the number printed under a barcode.
Frederik's by Meijer Vanilla Bourbon Trail Mix
- UPC
- 719283 357212
- Lot code
- 6069-1
- Expiration date
- 12/10/26
From the FDA notice
UPC 719283 357212; 12-9oz retail units per case.
Frederik's by meijer Vanilla Bourbon Trail Mix, packed in plastic retail-sized black bag NET WT 9 OZ (255g).
On the back of the bag is both lot number and a stamped expiration date.
Recall details
- Company began the recall
- Company
- Ferris Coffee and Nut Company, Inc.Grand Rapids, Michigan
- Hazard
- Undeclared wheat
- Risk
Moderate risk
Eating it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98811
- Recall number
- H-0774-2026
- Quantity recalled
- 125 cases (12-9oz retail units/case)
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Announced by the company
Listed on Recall Canary
Classified by FDA
Added to FDA's Enforcement Report
In FDA's weekly enforcement report
Recall ended
Archived
