FDA Device Intelligence
HomeRANDOX LABORATORIES LIMITED › C4

C4

RANDOX LABORATORIES LIMITED · Model CM3846 · UDI-DI 05055273201628

DBI Prescription
1
510(k) clearances
1
Adverse events
2
Recalls
32
Facilities

Description

A Complement C4 test system is a device intended for the quantitative in vitro determination of Complement C4 concentration in serum

Recalls

DateFirmReason
2020-08-27Roche Diagnostics Operations, Inc.Roche has confirmed customer complaints of low quality (QC) recovery and invalid calibrations for the identified products. A discoloration (yellow color) was observed and is the re
2018-05-16Abbott Laboratories, IncAn update to the Reagents and Specimen Collection and Handling/Preparation for Analysis sections of the IFU was required due to different issues with the various products.

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.