Recall Z-2557-2019
Randox Laboratories Ltd. · initiated July 25, 2019
Class III – products unlikely to cause any adverse health reaction but that violate FDA labeling or manufacturing laws
Product
Randox Urinalysis Control Level 2 (IVD) Ref: UC5034 - Product Usage: Product is intended for in vitro diagnostic use in the quality control of urine test strips.
Codes / lots: Lot: 1020UC Exp. Date: 28 May 2020
Reason for recall
Analyte range for Leukocytes for use with the Siemens Multistix method is incorrect. The range was corrected to NEGATIVE to 3+.
FDA-determined cause: Under Investigation by firm
Action taken
Randox Laboratories notified the distribution center USA by letter dated July 17, 2019 The distributor contacted the customer directly via email on July 25, 2019. The notification states: reason for recall, health risk and action to take: Discard current revision of the Value Sheet and replace with the revised copy available at www.randox.com " Discuss the contents of this notice with your Medical Director. Review results generated with the affected batches in line with the clinical profile of the patient. " Please retain this letter with your laboratory records and forward this letter to those who may have received this product. " Complete and return the response form 12187-QA to technical.services@randox.com within five working days.
Details
- Recall number
- Z-2557-2019
- Initiated
- July 25, 2019
- Terminated
- December 3, 2020
- Product code
- JJW – Urinalysis Controls (Assayed And Unassayed)
- Quantity
- 1 kit
- Distribution
- US Nationwide distribution including the states of IN, WV.
- Recalling firm
- Randox Laboratories Ltd., Crumlin, North