FDA Recall Open, Classified

Clinical Chemistry Calibration Serum (Catalog number Cal2351) that is 20x5ml lyophilized human based serum covering 38 commonly used clinical chemistry tests.

Recall: Z-1759-2024 · Initiated March 5, 2024

Recall

Recall Number
Z-1759-2024
Event Number
94358
Firm
Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland
FEI Number
1000361607
Product Code
JIX
Status
Open, Classified
Root Cause
Process design
Initiated
March 5, 2024
Posted
May 3, 2024

Description

Clinical Chemistry Calibration Serum (Catalog number Cal2351) that is 20x5ml lyophilized human based serum covering 38 commonly used clinical chemistry tests.

Reason

Randox Laboratories has identified that Inorganic Phosphate in Calibration Serum Level 3, CAL2351 & CAL10388, is running with a negative bias on RX Series instruments compared to other methods.

Action

Consignees were emailed a Medical Device Correction notice dated 3/5/2024 instructing them to discuss the contents of the notification with their facility's Medical Director if affected units have been used, replace the IFU for affected devices with the one provided with the notification, and complete and return the provided response form by email to technical [email protected] within five working days. Updated IFUs can be accessed at www.randox.com and questions can be directed to [email protected].

Distribution

Domestic: Nationwide Distribution.

Quantity

80,366 units (US: 242 units; OUS: 80,094 units)