FDA Device Intelligence
HomeRESEARCH AND DIAGNOSTIC SYSTEMS, INC. › Research and Diagnostic Systems

Research and Diagnostic Systems

RESEARCH AND DIAGNOSTIC SYSTEMS, INC. · Model RI003 · UDI-DI 00815762021237

JPK Prescription
10
510(k) clearances
93
Adverse events
16
Recalls
31
Facilities

Description

R&D Retic-I: 9 x 3mL TriPack Tubes (3 each Level 1,2,3)

Recalls

DateFirmReason
2022-11-07R & D Systems, Inc.For one lot of CBC-3D Hematology Control, the Normal Level may exhibit hemolysis or deterioration due to microbial contamination.
2021-10-05Primus Corporation dba Trinity BiotechThe Control Level I material value was showing results exceeding the upper limit of the acceptable range after a period of three (3) months. The unacceptable Control Level 1 value
2021-10-05Primus Corporation dba Trinity BiotechThe Control Level I material value was showing results exceeding the upper limit of the acceptable range after a period of three (3) months. Additionally, per the firm, the unacce
2021-01-25Medline Industries IncProduct was compromised during shipment.
2020-10-05Becton, Dickinson and Company, BD BiosciencesRecent product complaints showing an unexpected cell population exhibiting dim CD3 expression that may result in inaccurate results gating.
2013-02-24Clinical Diagnostic SolutionsElevated MCV results on the 1311-682, 1311-683, and 1311-684 lots.
2012-09-14Horiba Instruments, Inc dba Horiba MedicalHORIBA Medical Irvine Technical Support received reports from some customers that have experienced high recover values for Hemoglobin when using Minotrol 16 lot #MX090 (Level High)
2011-03-24Clinical Diagnostic SolutionsClinical Diagnostic Solutions, Inc. in Plantation, FL recalled Boule Con Diff US Tri Pack (Product Part 501-605, Lot #1102-575 and 1102-576; Product Part 501-607, Lot #1102-576; an
2011-03-24Clinical Diagnostic SolutionsClinical Diagnostic Solutions, Inc. in Plantation, FL recalled Boule Con Diff US Tri Pack (Product Part 501-605, Lot #1102-575 and 1102-576; Product Part 501-607, Lot #1102-576; an
2011-03-24Clinical Diagnostic SolutionsClinical Diagnostic Solutions, Inc. in Plantation, FL recalled Boule Con Diff US Tri Pack (Product Part 501-605, Lot #1102-575 and 1102-576; Product Part 501-607, Lot #1102-576; an

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.