FDA Device recall Z-0201-2024
RX Modena-IVD Clinical Chemistry Analyser Catalog Number: RX9000
- FDA Device
- Class II
- ongoing
- Published 2023-11-08
On 2023-11-08 the FDA classified a Class II recall of RX Modena-IVD Clinical Chemistry Analyser Catalog Number: RX9000 by Randox Laboratories, citing RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for Auto reruns, not meeting sample re-run conditions when samples are above or below assay range and may….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0201-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-09-06 |
| Published | 2023-11-08 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Randox Laboratories |
| Distribution | US |
Product
RX Modena-IVD Clinical Chemistry Analyser Catalog Number: RX9000
Reason
RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for Auto reruns, not meeting sample re-run conditions when samples are above or below assay range and may result i issues with the re-run feature conditions when incorrectly. Potential to report incorrectly.
Identifiers
| code_info | GTIN: 05055273214963 Lot/Batch Number: |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0201-2024%22
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