FDA Device Intelligence
HomeRoche Diagnostics GmbH › Tina-quant Antistreptolysin O

Tina-quant Antistreptolysin O

Roche Diagnostics GmbH · Model 08105472190 · UDI-DI 07613336133545

GTQ Prescription
10
510(k) clearances
5
Adverse events
4
Recalls
36
Facilities

Recalls

DateFirmReason
2008-11-18Remel, IncThese lots may exhibit false positive reactions with strains of Staphylococcus epidermidis that may result in the mis-identification of Staphylococcus aureus.
2007-08-08BD Diagnostic Systems / Lee LaboratoriesIncorrect result: The product exhibited decreased fluorescence when testing with the homologous control organism.
2006-07-25Roche Diagnostics Corp.The vial containing the R2 reagent is labeled as R1 reagent and if placed in the R1 slot of the analyzer, erroneous results will be obtained. (extremely low patient and control res
2003-12-17Beckman Coulter IncThe ASO (MPE) assayed in Buffer cannot be programmed or calibrated using Array Calculator 5.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.