FDA recall record

Beckman Coulter UA WIN 10 Kit, Catalog Number C52900, in-vitro diagnostic device, urine recall — FDA Z-1599-2023

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…

Class IIclassification
Z-1599-2023official record ID
May 24, 2023report date

Recall record at a glance

Official recordZ-1599-2023
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmBeckman Coulter, Inc.
Report dateMay 24, 2023
Recall initiation dateApr 5, 2023
Quantity306 units
LocationMiami, FL, United States

Official product description

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

Why the product was recalled

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 information

Worldwide Distribution

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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