RX daytona plusRecalls & reported problems across all models
Randox Laboratories Limited · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
2 open recalls name at least one RX daytona plus model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 2
We found 2 models of RX daytona plus by Randox Laboratories Limited in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
2 FDA recall records name at least one of these models by its device identifier, 2 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
RX daytona plus recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Sep 6, 2023Open, Classified
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.
Z-0199-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Sep 6, 2023Open, Classified
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.
Z-0198-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
RX daytona plus models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- RX daytona plus RX4040Analyzer, Chemistry (Photometric, Discrete), For Clinical Use1 recall0 reports
- RX daytona plus RX4041Analyzer, Chemistry (Photometric, Discrete), For Clinical Use1 recall0 reports
Other Randox Laboratories Limited products
All Randox Laboratories Limited devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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