Lower riskFood recall · FDA · Published July 9, 2019
DaVinci Labs Omega 3 Supplement Mislabeling Risk
FoodScience Corporation recalls DaVinci Labs Omega 3-1,000 supplement due to mislabeling and undeclared allergen. Consumers should check product details and contact for guidance.
FoodScience Corporation is recalling DaVinci Laboratories of Vermont's Omega 3-1,000 supplement because it's mislabeled and contains an undeclared allergen. This could cause allergic reactions in people sensitive to the allergen. Read more at govinfonow.com/recall/16983-davinci-labs-omega-3-supplement-mislabeling-risk.
“DaVinci Labs Omega 3 Supplement Mislabeling Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16983-davinci-labs-omega-3-supplement-mislabeling-risk. Based on FDA recall #F-1595-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1595-2019%22&limit=1).
The FDA announced on July 9, 2019, that FoodScience Corporation voluntarily recalled DaVinci Laboratories of Vermont Omega 3-1,000 dietary supplements due to mislabeling and an undeclared allergen. Consumers should stop using the product immediately.
How to tell if you have it
DaVinci Laboratories of Vermont Omega 3-1,000 in a white bottle labeled as Dim Plex, 60 count
UPC Code 026664273161
Lot Code: 35532200
EXP: 05/2022
The hazard
The dietary supplement was mislabeled and contained an undeclared allergen. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show FoodScience Corporation has one other recall on record since November 8, 2013. That previous recall involved a chloramphenicol risk in Cyb Zyme Dietary Supplement recalled on 2013-11-08. Other recent recalls of similar products include Vital Nutrients Aller-C Recall (2026-03-27), Imu-Tek Immuno-5 Colostrum Powder Recall (2025-11-25), and Genepro Whey Protein Recall (2025-11-12).
How to tell if you have this one
Check for a white bottle labeled 'Dim Plex', 60-count, UPC 026664273161, and lot code 35532200 with an expiration date of May 2022.
Brand
DaVinci Laboratories of Vermont
Product
DaVinci Laboratories of Vermont Omega 3-1,000 in a white bottle labeled as Dim Plex, 60 count UPC Code 026664273161
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the white bottle labeled 'Dim Plex', 60-count, UPC 026664273161, and lot code 35532200 with expiration date May 2022.
Where it went and when
Where it was distributed
Distributed in 18 states, and outside the U.S.
Listed by the agency
Not listed
FDA distribution: “Product distributed to customers in the following states: PA< IN, CA, NH, VT, MD, MI, MN, NY, LA, CT, OR, MO, AZ, OH, FL, KS, IL. There is one International customer in Tokyo, Japan.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, Connecticut, Florida, Illinois, Indiana, Kansas, Louisiana, Maryland, Michigan, Minnesota, Missouri, New Hampshire, New York, Ohio, Oregon, Pennsylvania, Vermont.
Recall timeline
FDA terminated this recall 3 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-1595-2019 (July 9, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1595-2019 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 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.