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

VITROS

ORTHO-CLINICAL DIAGNOSTICS, INC. · Model 6800120 · UDI-DI 10758750000593

JGP Prescription
5
510(k) clearances
1
Adverse events
2
Recalls
9
Facilities

Description

VITROS Chemistry Products UPRO Slides

Recalls

DateFirmReason
2016-12-08Ortho-Clinical DiagnosticsThere is a potential for variable negatively and positively biased urine protein results using VITROS UPRO Slides.
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.