FDAFDA · Food and drugs·Recall number Z-1785-2019
Liquid Cardiac Control, Model Nos. CQ5051, CQ5052, CQ5053
Published June 26, 2019 · Recall initiated: March 11, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Randox Laboratories Ltd.
- Distributor
- Product distributed to CA, DE, WV, and Puerto Rico.
- Lot
- lots 4243CK, 4244CK, 4245CK.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- Ireland
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