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Recall Observatory FDA recall evidence

Device product

Randox RX Imola Analyser with ISE, Catalog Numbers RX4900, RX4900R

Z-2013-2021

April 28, 2021

Class II

Product summary

Firm
Randox Laboratories Ltd.
Event
Event 88098
Status
Terminated
Classification
Class II
Quantity
50 kits
Official record key
device-enforcement:Z-2013-2021

Official wording

Reason: An issue was identified where the software froze during processing of commands, which resulted in no results displayed.

Code information: GTIN 05055273206104, Serial Numbers: 7201-0423 7201-0417 7201-0353 7201-0776 7201-0367 7201-0921 7201-0982 7201-0977 7201-0970 7201-0950 7201-0924 7201-0919 7201-0901 7201-0849 7201-0827 7201-0799 7201-0801 7201-0768 7201-0606 7201-0562 7201-0535 7201-0531 7201-0381 7201-0112 7201-0231 7201-0275 7201-0299 7201-0319 7201-0343 7201-0348 7201-0391 7201-0514 7201-0515 7201-0540 7201-0605 7201-0616 7201-0840 7201-0533 7201-0932 7201-0943 7201-0513 7201-0482 7201-0960 7201-0882 7201-0434 7201-0607 7201-0768 7201-0961 7201-0980 7201-0994

Distribution pattern: US Nationwide Distribution and Puerto Rico.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    issue was identified where the software