Randox Laboratories Ltd.: Medical Device Recall in 2019 - (Recall #: Z-1785-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: March 11, 2019

Date Posted: June 26, 2019

Recall Number: Z-1785-2019

Event ID: 82400

Reason for Recall:

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.

Status: Terminated

Product Quantity: 11420 kits

Code Information:

lots 4243CK, 4244CK, 4245CK.

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated