This page has been archived on the Web
Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.
Sensodyne Rapid Relief (2015-07-13)
- Starting date:
- July 13, 2015
- Posting date:
- July 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-54250
Affected Products
- Sensodyne Rapid Relief
Reason
The impacted products are being recalled as a precautionary measure because they may contain wood fragments.
Depth of distribution
Retailers
Affected products
Sensodyne Rapid Relief
DIN, NPN, DIN-HIM
NPN 80026197Dosage form
Paste
Strength
- Strontium acetate hemihydrate 8.0 % w/w
- Sodium fluoride 0.23% w/w
Lot or serial number
- 3G161
- 3J051
- 3J121
- 3M271
- 3N031
- 4B241
- 4B281
- 4C061
- 4C211
- 4C241
- 4E291
- 4F011
- 4G081
- 4G261
-
4H301
Companies
- Recalling Firm
-
GlaxoSmithKline Inc.
7333 Mississauga Road
Mississauga
L5N 6L4
Ontario
CANADA
- Marketing Authorization Holder
-
GlaxoSmithKline Inc.
7333 Mississauga Road
Mississauga
L5N 6L4
Ontario
CANADA