FDA Recall Open, Classified

Liquid Assayed Chemistry Control Premium Plus Level 3, Catalog Number LAE4215

Recall: Z-2609-2023 · Initiated August 3, 2023

Recall

Recall Number
Z-2609-2023
Event Number
92912
Firm
Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland
FEI Number
1000361607
Product Code
JJY
Status
Open, Classified
Root Cause
Under Investigation by firm
Initiated
August 3, 2023
Posted
September 19, 2023

Description

Liquid Assayed Chemistry Control Premium Plus Level 3, Catalog Number LAE4215

Reason

there has been a transcription error in the Instructions for Use (IFU) for the Liquid Assayed Chemistry Control Premium Plus Level 3. For Caeruloplasmin, the one and two standard deviation values printed on the sheet are incorrect, which may lead to misreporting patient results. Target and range values are correct, and risk is mitigated; most clinical labs will use the target and range values in clinical practice.

Action

A Medical Device Correction notification letter dated 8/3/23 was sent to customers. Action to be taken: " Review Quality Control data generated using the affected lot. " 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. 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.

Distribution

US States: GA, OH, OR, PA, TX, VA

Quantity

66 kits