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: 2019-12-27
Summary
-
Product:
- U-Dream Lite Capsule
- U-Dream Full Capsule
- U-Dream Lite Capsule
- 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
-
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