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Hyper FX (2014-01-14)
- Starting date:
- January 14, 2014
- Posting date:
- January 28, 2014
- 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-37731
Recalled Products
Hyper FX
Reason
The product was removed because the amount of caffeine (665 mg/day) in the presence of synephrine exceeds the acceptable amount.
Depth of distribution
Retailers in Canada
Affected products
Hyper FX
DIN, NPN, DIN-HIM
No Market Authorization
Dosage form
Powder
Strength
Synéphrine 24 mg/day
Cafeine 665 mg/day
Lot or serial number
21454A
20584A
21434A
20454A
20614A
21424A
20123A
234940A
Companies
- Recalling Firm
-
Empire Health Distribution
585 Fernand Poitras
Terrebonne
J6Y 1Y5
Quebec
CANADA
- Marketing Authorization Holder
-
Not Applicable