Calibration Serum Level 3. CAL 3, REF CAL2351. Human Assayed Multi-Sera Level 2 (HN1530) Human Assayed Multi-Sera Level 3 (HE 1532)
FDA Recall Z-0751-2024 · Posted 2024-01-18
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Recalling FirmRandox Laboratories Ltd.
Recall StatusOpen, Classified
Product CodeJIX
Date Initiated2023-11-13
Reason for Recall
There have been transcription errors on the Instructions For Use (IFU) of the Calibration Serum
Level 3 (CAL2351 lot 1260UE, 1262UE and 1315UE) for target values of Bilirubin and Triglycerides, on the
IFU of Human Assayed Multi-Sera Level 2 (HN1530) for TBIC taget value and on IFU of Human Assayed
Multi-Sera Level 3 (HE 1532) for Lipase target value.
Firm Action
On November 20, 2023, the firm notified customers via Medical Device Correction letter.
The letter consisted of three parts. This recall record covers the third part, which concerned transcription errors in the Instructions for Use (IFU) for the above listed products. Customers should discard all copies of the IFUs and download the latest versions from www.randox.com.
Customers should discuss the contents of the recall notice with their Medical Director if they have used the incorrect target value for any of the affected products.
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide distribution.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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