ADVIA Chemistry GGT ReagentsRecalls & reported problems across all models
Siemens Healthcare Diagnostics Inc. · 2 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names at least one ADVIA Chemistry GGT Reagents 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
- 1
We found 2 models of ADVIA Chemistry GGT Reagents by Siemens Healthcare Diagnostics Inc. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
1 FDA recall record name at least one of these models by its device identifier, 1 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
ADVIA Chemistry GGT Reagents 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.
- Nov 23, 2020Class IIOpen, Classified
Gamma-Glutamyl Transferase (GGT) Reagent Low End Repeatability-Imprecision. Reagent may demonstrate a coefficient of variation (%CV) outside of the performance data for repeatability (within-run) listed in the Instructions For Use (IFU) on some analyzers.
Z-0721-2021 · Root cause: Device Design · names 2 of these models · Recall details · FDA record ↗
ADVIA Chemistry GGT Reagents models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- ADVIA® Chemistry GGT Reagents 10316298ELECTROPHORETIC, GAMMA-GLUTAMYL TRANSPEPTIDASE ISOENZYMES1 recall0 reports
- ADVIA® Chemistry GGT Reagents 10309495ELECTROPHORETIC, GAMMA-GLUTAMYL TRANSPEPTIDASE ISOENZYMES1 recall0 reports
Other Siemens Healthcare Diagnostics Inc. products
- Atellica IM TNIH2 models · 629 reports
- Dimension EXL 200 Integrated Chemistry System2 models · 516 reports · 1 recall
- Atellica IM CA 19-93 models · 121 reports · 3 recalls
- ADVIA Centaur XP Analyzer2 models · 269 reports
- ADVIA Centaur CA 19-92 models · 124 reports · 2 recalls
- Atellica IM eE23 models · 65 reports · 3 recalls
- RAPIDPoint 500 Measurement Cartridge4 models · 3 reports · 4 recalls
- ADVIA Centaur eE23 models · 22 reports · 3 recalls
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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