Lower riskFood recall · FDA · Published July 26, 2021
Monfefo Turmeric Shots Recall: Product Not Made to Specs
Monfefo recalls 12-packs and single shots of turmeric juice due to manufacturing defects. Check UPCs and expiration dates listed for affected products.
“Monfefo Turmeric Shots Recall: Product Not Made to Specs.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14297-monfefo-turmeric-shots-recall-product-not-made-to-specs. Based on FDA recall #F-0860-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0860-2021%22&limit=1).
Monfefo LLC voluntarily recalled its Monfefo brand Turmeric Shot on July 26, 2021, according to the FDA. The product was not manufactured according to specifications. Owners should contact the company for a refund.
How to tell if you have it
Brand: Monfefo
Product: Turmeric Shot; 2oz; Cold Pressed Juice Blend; packaged in glass bottle
The FDA stated the product was not manufactured according to specifications. The recall is classified as Class II.
Context
GovInfoNow's records show other recent recalls of similar products include Imu-Tek Colostrum-5 Powder Recall (2026-02-24), Quten Turmeric Capsules Recall (2025-12-16), and Trafa Organic Moringa Leaf Powder Recall (2026-06-24).
How to tell if you have this one
Check for Monfefo Turmeric Shots with UPC 660002515441 (12-pack) or UPC 860002515410 (single shot). Products with expiration dates from August 2021 through September 2021 are affected.
Brand
Monfefo
Product
Monfefo brand Turmeric Shot; 2oz; Cold Pressed Juice Blend; packaged in glass bottle
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Details
Identify your Monfefo Turmeric Shot with the specific UPC numbers and expiration dates listed in the recall.
Where it went and when
Where it was distributed
Distributed in 18 states and D.C..
Listed by the agency
Not listed
FDA distribution: “NY, NJ, CT, TX, MD, DC, FL, ME, MA, VT, OH, PA, VA, GA, NC, SC, WI, CO, CA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Maine, Maryland, Massachusetts, New Jersey, New York, North Carolina, Ohio, Pennsylvania, South Carolina, Texas, Vermont, Virginia, Wisconsin.
Recall timeline
FDA terminated this recall 10 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0860-2021 (July 26, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0860-2021 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.