FDA recall record

Randox Urinalysis Control Level 2 (IVD) Ref: UC5034 - Product Usage: Product is intended for recall — FDA Z-2557-2019

Analyte range for Leukocytes for use with the Siemens Multistix method is incorrect. The range was corrected to NEGATIVE to 3+.

Class IIIclassification
Z-2557-2019official record ID
Oct 2, 2019report date

Recall record at a glance

Official recordZ-2557-2019
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmRandox Laboratories Ltd.
Report dateOct 2, 2019
Recall initiation dateJul 25, 2019
Quantity1 kit
LocationCrumlin (North), Ireland

Official product description

Randox Urinalysis Control Level 2 (IVD) Ref: UC5034 - Product Usage: Product is intended for in vitro diagnostic use in the quality control of urine test strips.

Why the product was recalled

Analyte range for Leukocytes for use with the Siemens Multistix method is incorrect. The range was corrected to NEGATIVE to 3+.

Distribution information

US Nationwide distribution including the states of IN, WV.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.