Official recall record
DiaClon ABO/D+ Reverse-Group
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-04-09
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Bio-Rad Laboratories would like to inform its customers that user of IH-1000 and/or IH-500 may notice a slight increase in cases of visually interpreted "4+" reactions returned as double population "DP" by these instruments when using the DiaClon ABO/D+ Reverse-Group cards. Recall start date: March 27, 2024
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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