Home › INOVA DIAGNOSTICS, INC. › QUANTA Flash® dsDNA Reagents
QUANTA Flash® dsDNA Reagents
INOVA DIAGNOSTICS, INC. · Model 701178 · UDI-DI 08426950624646
LSW
Prescription
1
510(k) clearances
5
Adverse events
1
Recalls
8
Facilities
Description
1 QUANTA Flash dsDNA Reagent Cartridge
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-12-14 | Phadia US Inc | Decreased values for EliA ANA Positive Control when using the EliA dsDNA Well lot BFA37/0142 may potentially cause false positive results (increase in patient test results). |
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 docsData 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.
