FDA Device Intelligence
Home › ORTHO-CLINICAL DIAGNOSTICS, INC. › VITROS

VITROS

ORTHO-CLINICAL DIAGNOSTICS, INC. · Model 8046872 · UDI-DI 10758750004270

DMT Prescription
8
510(k) clearances
2
Adverse events
1
Recalls
11
Facilities

Description

VITROS Chemistry Products ALC Slides

Recalls

DateFirmReason
2013-06-12Ortho-Clinical DiagnosticsOrtho Clinical Diagnostics is recalling Slide Dispense cartridges used with some VITROS Chemistry Product Slides due to slide dispense issues.

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.