Magna Pure 24 Instrument (2018-05-14)
- Starting date:
- May 14, 2018
- Posting date:
- June 1, 2018
- 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-66904
Affected products
Magna Pure 24 Instrument
Reason
There is a potential for cross-contamination when using specific protocols (Pathogen 200 version 1 and Pathogen 1000 version 1) on the MagNA Pure 24 System.
Affected products
Magna Pure 24 Instrument
Lot or serial number
Pathogen 1000 version I
Pathogen 200 version I
Model or catalog number
07290519001
Companies
- Manufacturer
-
Roche Diagnostics GMBH
Sandhoferstrasse 116
Mannheim
68305
GERMANY