Home › Siemens Healthcare Diagnostics Products GmbH › LA 2 Confirmation Reagent
LA 2 Confirmation Reagent
Siemens Healthcare Diagnostics Products GmbH · Model 10873902 · UDI-DI 00630414639451
2
510(k) clearances
4
Adverse events
1
Recalls
12
Facilities
Description
LA 2 Confirmation Reagent. Phospholipid-rich DRVV reagent for the specific correction of Lupus Anticoagulants
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-02-28 | American Diagnostica, Inc. | Stability of product not assured. An increase of clotting time for both normal and abnormal plasmas |
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.