MAGNESIUM (Mg) MG3880Recalls & reported problems
Randox Laboratories Limited · Class 1
- 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. How this data works · Data updated Oct 13, 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-0546-2021 · Root cause: Under Investigation by firm · 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
- Dimension® Flex® reagent cartridge MG 10444963Siemens Healthcare Diagnostics Inc. · PHOTOMETRIC METHOD, MAGNESIUM1 recall0 reports
- MAGNESIUM (Mg) MG8326Randox Laboratories Limited · 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.