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Rubicon Holdings Corp.

Recall notice from Health Canada: Simply Bare Organics BC Organic Blue Dream Pre-Rolls

Not yet reviewed by our editors. This entry reports what the cited sources say; it may change as we check it. How we check

This entry is about Canada — not the country you picked in the header.

According to Health Canada, May 28, 2026 · Read the source

Where
Canada
First reported
Last checked

Summary

Rubicon Holdings Corp. recalled Simply Bare Organics BC Organic Blue Dream Pre-Rolls, according to a Health Canada notice dated May 28, 2026 (RA-82131). The notice states: The affected products contain the wrong pre-rolls. Therefore, the labels for the affected products have incorrect cannabinoid values.

The notice reports 2,304 units sold. To date, Rubicon Holdings Corp. has received 8 complaints from the retail-level about the recalled lot, none of which involved an adverse reaction. Health Canada has not received any complaints or adverse reaction reports. Check to see if your products are affected.

What the source found

  • Product named in the notice: Simply Bare Organics BC Organic Blue Dream Pre-Rolls
  • Issue category on the notice: Labelling and packaging
  • Stated reason: The affected products contain the wrong pre-rolls. Therefore, the labels for the affected products have incorrect cannabinoid values.
  • Units reported sold: 2,304
  • To date, Rubicon Holdings Corp. has received 8 complaints from the retail-level about the recalled lot, none of which involved an adverse reaction. Health Canada has not received any complaints or adverse reaction reports.

Products named

  • Simply Bare Organics BC Organic Blue Dream Pre-Rolls

Timeline

  1. Recall notice published by Health Canada (RA-82131)

Sources

  1. Regulator

Wording on this page follows the sources. Found an error? See the corrections process in our editorial policy.

Status notes

[dataset] Health Canada Recalls and Safety Alerts open data (HCRSAMOpenData.csv), category Cannabis and related cannabis recalls, retrieved 2026-09-30; licensed-producer recall, not an allegation of wrongdoing.

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