This page has been archived on the Web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.
ID-PAPAIN (2016-04-25)
- Starting date:
- April 25, 2016
- Posting date:
- May 16, 2016
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-58364
Affected products
- ID-PAPAIN
Reason
Following customer complaints, DiaMed GMBH was able to confirm that the lot of ID-Papain above show a decrease in enzyme activity, leading to uninterpretable results.
Affected products
-
ID-PAPAIN
Lot or serial number
- 06311.54.1
Model or catalog number
- 5510
Companies
- Manufacturer
-
Diamed GMBH
Pra Rond 23
Cressier FR
1785
SWITZERLAND