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Diaclon abo d+ reverse-group
Official notice
9 Apr 2024
Last checked
9 Apr 2024
An official Health Canada notice concerns Diaclon abo d+ reverse-group. 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 Published 2024-04-09.
What to do now
Contact CDGCANADA_TECHNICALSERVICES@BIO-RAD.COM if you require additional information.
Recall number
75368
Official notice
2024-04-09
The hazard
The hazard
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
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
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Affected products
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Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Manufacturer
Phone
Brand: Bio-rad Medical Diagnostics, Diaclon Abo D+ Reverse-group.
Source & status
Source & status
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Tier
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Classification
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Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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