ClearanceBrief
Recall Z-1596-2023 ยท KQO Automated Urinalysis System

Beckman Coulter, Inc.

iQ200 Series Urine Microscopy Analyzer: a) iQ 200 Select, Part Numbers C10684 and 700-3345; b) iQ 200 Elite, Part Numbers C10683 and 700-3375; in-vitro diagnostic device, urine analysis, c) iQ200 Select 1500, Part Number 700-3347, d) iQ200 Sprint, Part Number 700-3325

DateMay 17, 2023 (initiated Apr 5, 2023)
StatusOpen, Classified
ReasonBeckman Coulter has become aware of an intermittent issue in which the optional flag Previous Sample Had Sperm was enabled but not displayed so that a carryover event could have been investigated.
Root causeUnder Investigation by firm
ActionBeckman Coulter issued an URGENT MEDICAL DEVICE RECALL notice to its consignees on 04/05/2023 by mail. The notice explained the issue and the hazard and requested the following actions be taken: "Examine your specimen settings to determine if the optional 'Sperm Present' and 'Previous Sample Had Sperm' flags are enabled. If disabled, no further action is needed by your laboratory. If enabled, follow the actions below If the presence of sperm is identified: Review the previous specimen for the presence of sperm. Follow recommendations under Previous Sample Had Sperm in the iQ200 Series
Quantity1068 units
DistributionWorldwide Distribution
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K022774IQ 200 SYSTEM
Intl. Remote Imaging Systems, Oct 21, 2002
K093861IQ 20 SERIES ANALYZER, IQ 200 SERIES SYSTEM, NAD IQ LAMINA CRADLE
Iris International, Inc., Feb 5, 2010
K210127iQ200 System, iChemVELOCITY Automated Urine Chemistry System
Beckman Coulter, Inc., Jul 2, 2021