FDA recall Z-1599-2023

Product

UA WIN 10 Kit, Catalog Number C52900, in-vitro diagnostic device, urine analysis

Reason for recall

Beckman 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.

Distribution

Worldwide Distribution

Key facts

Status

Ongoing

Initiation date

2023-04-05

Report date

2023-05-24

Voluntary/Mandated

Voluntary: Firm initiated

Location

Miami, FL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1599-2023