Randox RX Imola Analyser with ISE, Catalog Numbers RX4900, RX4900R
FDA Recall Z-2013-2021 · Posted None
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Recalling FirmRandox Laboratories Ltd.
Recall StatusTerminated
Product CodeCEM
Date Initiated2021-04-28
Date Terminated2021-12-03
Product Quantity50 kits
Reason for Recall
An issue was identified where the software froze during processing of commands, which resulted in no results displayed.
Firm Action
Urgent Medical Device Correction letters dated 4/28/21 were sent to customers.
Action to be taken:
" Discuss the contents of this notice with your Medical Director.
" Complete and return the response form 12187-QA to [email protected] within five working days.
" Please contact your local service provider to arrange for the software update to be performed .
"Transmission of Field Safety Notice: Send a copy of the FSN to all affected customers and to those who need to be aware within your organisation.
Please accept our apologies for any inconvenience caused. Thank you for your patience and understanding. If you have any questions or concerns please contact Randox Technical Services.
Local Contact Information
USA
Randox Laboratories-US, Ltd.
515 Industrial Boulevard
Kearneysville
West Virginia, 25430
Tel: +1 304 728 2890 Toll Free 866 4 RANDOX
Email: [email protected]
Puerto Rico
Clinical Diagnostics of P.R. LLC
Carr. 887km 0.6,
Carolina Commercial Park
Local B-2 Carolina, Puerto Rico
Tel: 1-787-701-7000
Email: [email protected]
Root Cause
Software design
Distribution Pattern
US Nationwide Distribution and Puerto Rico.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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