International safety notice
RA-37591 D-10 Haemoglobin Testing System - Dual Program (HBA2/E/AIC) (2013-12-19)
CAN / Health Canada · CAN · Jan 17, 2014
Key facts
| Title | RA-37591 D-10 Haemoglobin Testing System - Dual Program (HBA2/E/AIC) (2013-12-19) |
|---|---|
| Regulator | CAN / Health Canada |
| Country | CAN |
| Brand | D-10 Haemoglobin Testing System - Dual Program (HBA2/E/AIC) | |
| Manufacturer | Bio-Rad Laboratories Clinical Diagnostics Group 4000 Alfred Nobel Drive Hercules 94547 California UNITED STATES |
| Models | 64002239, 64000888, 64000331, 220-0201 |
| Event type | Recall |
| Date | Jan 17, 2014 |
| Regulator page | recalls-rappels.canada.ca |
At a glance
- Yes Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1