MAGNESIUM (Mg) MG8326Recalls & reported problems
Randox Laboratories Limited · Class 1
All models of MAGNESIUM (Mg) (2)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Recalls naming this device
- Nov 13, 2020Terminated
Failing to meet the linearity performance claims quoted on the kit inserts-The linearity is reduced by approximately -30% for Serum/ Plasma and -50% for Urine
Z-0547-2021 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Other Photometric Method, Magnesium devices
- ARCHITECT 7D70-21Abbott Laboratories · PHOTOMETRIC METHOD, MAGNESIUM1 recall37 reports
- ARCHITECT 7D70-31Abbott Laboratories · PHOTOMETRIC METHOD, MAGNESIUM1 recall16 reports
- Dimension Vista® Flex® reagent cartridge MG 10445158Siemens Healthcare Diagnostics Inc. · PHOTOMETRIC METHOD, MAGNESIUM1 recall5 reports
- MAGNESIUM (Mg) MG3880Randox Laboratories Limited · Photometric Method, Magnesium1 recall0 reports
- Dimension® Flex® reagent cartridge MG 10444963Siemens Healthcare Diagnostics Inc. · PHOTOMETRIC METHOD, MAGNESIUM1 recall0 reports
- ARCHITECT 03P6822Abbott GmbH · PHOTOMETRIC METHOD, MAGNESIUM43 reports
- Alinity 08P1934Abbott Ireland · PHOTOMETRIC METHOD, MAGNESIUM30 reports
- ARCHITECT 03P6824Abbott Ireland · PHOTOMETRIC METHOD, MAGNESIUM22 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- 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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