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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 83292

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
July 09, 2019
Product types
Food
Classifications
Class II
Statuses
Terminated
Recalling firm wording
FoodScience Corporation

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 1

DaVinci Laboratories of Vermont Omega 3-1,000 in a white bottle labeled as Dim Plex, 60 count UPC Code 026664273161

F-1595-2019
Recall number
F-1595-2019
Initiated
July 09, 2019
Classification
Class II
Status
Terminated
Recalling firm
FoodScience Corporation
Quantity
256 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeled
Undeclared allergen reason.undeclared_allergen · v1.0.0
undeclared allergen

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Dietary supplement mislabeled, undeclared allergen.

Code information

Lot Code: 35532200 EXP: 05/2022

Distribution pattern

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.