FDA recall record

Randox Laboratories Liquid Cardiac Control, Model Nos recall — FDA Z-1785-2019

Customers may observe a decrease in recovered concentration with regards to NTproBNP in the Liquid Cardiac Control lots identified, on the Siemens…

Class IIclassification
Z-1785-2019official record ID
Jun 26, 2019report date

Recall record at a glance

Official recordZ-1785-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmRandox Laboratories Ltd.
Report dateJun 26, 2019
Recall initiation dateMar 11, 2019
Quantity11420 kits
LocationCrumlin (North), N/A, Ireland

Official product description

Liquid Cardiac Control, Model Nos. CQ5051, CQ5052, CQ5053

Why the product was recalled

Customers may observe a decrease in recovered concentration with regards to NTproBNP in the Liquid Cardiac Control lots identified, on the Siemens Dimension EXL LOCI.

Distribution information

Product distributed to CA, DE, WV, and Puerto Rico.

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: 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.

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