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Ultra D-Tox (2015-04-13)
- Starting date:
- April 13, 2015
- Posting date:
- April 16, 2015
- Type of communication:
- Drug Recall
- Subcategory:
- Natural health products
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Product Safety
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-52949
Recalled Products
Ultra D-Tox
Reason
Lead levels exceed acceptable daily limits when 2 or more capsules are taken.
Depth of distribution
Retailers
Affected products
Ultra D-Tox
DIN, NPN, DIN-HIM
NPN 80035567
Dosage form
Capsule
Strength
- Allium sativum 20 mg
- Aloe vera 5 mg
- Apium graveolens var. dulce 5 mg
- Bentonite 300 mg
- Chlorella Pyrenoidosa 60 mg
- Hordeum vulgare 5 mg
- Lacobacillus acidophilus 250 million cfu
- Linum usitatissimum 5 mg
- Magnesium 18 mg
- Mentha x piperita 5 mg
- Pimpinella anisum 5 mg
- Plantago ovata 10 mg
- Prunus spp. 5 mg
- Stem bromelain 3 mg
- Vitamin C 30 mg
Lot or serial number
- 50029524
- 4073613
Companies
- Recalling Firm
-
Douglas Laboratories of Canada (Importer)
490 Elgin Mills Road East
Richmond Hill
L4C 0L8
Ontario
CANADA
- Marketing Authorization Holder
-
Douglas Laboratories of Canada (Importer)
490 Elgin Mills Road East
Richmond Hill
L4C 0L8
Ontario
CANADA