U-Dream Product Recall (2019-12-20)

Starting date:
December 20, 2019
Type of communication:
Drug Recall
Subcategory:
Natural health products
Hazard classification:
Type I
Source of recall:
Health Canada
Issue:
Product Safety
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-71963

Last updated:

Summary

  • Product:
    1. U-Dream Lite Capsule
    2. U-Dream Full Capsule
  1. U-Dream Lite Capsule
  2. U-Dream Full Capsule

Reason

Affected lots contain an undeclared ingredient similar to one that is listed on the prescription drug list.

Depth of distribution

Retailers 

Affected products

  1. U-Dream Lite Capsule

DIN, NPN, DIN-HIM

NPN 80072688

Dosage form

Capsule

Strength

Eriobotrya japonica 75.0 mg
Hericium erinaceus 85.0 mg
L-Tryptophan 20.0 mg
Passiflora incarnata 100.0 mg
Rehmannia glutinosa 25.0 mg
Reynoutria multiflora 25.0 mg
Schisandra chinensis 75.0 mg
Ziziphus jujuba 45.0 mg

Lot or serial number

All lots

Companies

Recalling Firm
Puresource Inc.
5-5068 Whitelaw Road
Guelph
N1H 6J4
CANADA
Marketing Authorization Holder
Biotrade Canada Limited
2733 Countryside Place
Shawnigan Lake
V0R 2W2
British Columbia
CANADA

B. U-Dream Full Capsule

DIN, NPN, DIN-HIM

NPN 80072690

Dosage form

Capsule

Strength

Eriobotrya japonica 65.0 mg
Hericium erinaceus 85.0 mg
L-tryptophan 30.0 mg
Passiflora incarnata 110.0 mg
Rehmannia glutinosa 15.0 mg
Reynoutria multiflora 15.0 mg
Schisandra chinensis 85.0 mg
Ziziphus jujuba 45.0 mg

Lot or serial number

All lots

Companies

Recalling Firm
Puresource Inc.
5-5068 Whitelaw Road
Guelph
N1H 6J4
CANADA
Marketing Authorization Holder
Biotrade Canada Limited
2733 Countryside Place
Shawnigan Lake
V0R 2W2
British Columbia
CANADA