CLASS II Food recall · Reported 31 Jul 2019 · FDA Enforcement Report
DaVinci Laboratories of Vermont Omega 3- a white bottle recalled
FoodScience is recalling DaVinci Laboratories of Vermont Omega 3- a white bottle labeled as Dim Plex, distributed in 17 states. The recall was initiated on 9 Jul 2019 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1595-2019
- FDA event ID
- 83292
- Recalling firm
- FoodScience, Williston, VT
- Brand
- DaVinci Laboratories
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 9 Jul 2019
- FDA classified
- 23 Jul 2019
- Reported
- 31 Jul 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Undeclared Allergens
- Product category
- Fish Oil
Timeline
| 9 Jul 2019 | Recall initiated by company | |
| 23 Jul 2019 | Classified by FDA | +14 days |
| 31 Jul 2019 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Dietary supplement mislabeled, undeclared allergen.
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
DaVinci Laboratories of Vermont Omega 3-1,000 in a white bottle labeled as Dim Plex, 60 count UPC Code 026664273161
Where it was distributed
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.
ArizonaCaliforniaConnecticutFloridaIllinoisKansasLouisianaMarylandMichiganMinnesotaMissouriNew HampshireNew YorkOhioOregonPennsylvaniaVermont
Questions about this recall
Why was it recalled?
Dietary supplement mislabeled, undeclared allergen.
Which lots are affected?
Lot Code: 35532200 EXP: 05/2022
Where was it sold?
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.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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