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Autostat II Anti-ds-DNA

HYCOR BIOMEDICAL LLC · Model FGA01 · UDI-DI 00816879020014

LRM
10
510(k) clearances
109
Adverse events (2 deaths)
3
Recalls
14
Facilities

Description

96 well ELISA for the detection of anti-dsDNA antibodies in human serum

Recalls

DateFirmReason
2010-03-02Bio-Rad Laboratories IncThe firm received customer complaints of increased positivity rates associated with the Anti-dsDNA test kits.
2010-03-02Bio-Rad Laboratories IncThe firm received customer complaints of increased positivity rates associated with the Anti-dsDNA test kits.
2008-08-27Calbiotech IncThe recall has been initiated due to the "For Export Only" labeling found on some Calbiotech, Inc. ELISA kits. Although there is no potential health hazard related to this recall,

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.