Atellica IM eE2 11206250Recalls & reported problems
Siemens Healthcare Diagnostics Inc. · Estradiol (eE2) - Atellica IM - RGT 500T · Class 1
All models of Atellica IM eE2 (3)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- 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, 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, 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 18, 2026.
Recalls naming this device
- Mar 3, 2022Class IIOpen, Classified
Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
Z-1022-2022 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Other RADIOIMMUNOASSAY, ESTRADIOL devices
- Atellica IM eE2 10995561Siemens Healthcare Diagnostics Inc. · RADIOIMMUNOASSAY, ESTRADIOL1 recall61 reports
- Elecsys Estradiol III 6656021190Roche Diagnostics GmbH · RADIOIMMUNOASSAY, ESTRADIOL101 reports
- VIDAS® Estradiol II 30431-01Biomerieux SA · RADIOIMMUNOASSAY, ESTRADIOL2 recalls0 reports
- IMMULITE® 2000 Systems E2 Estradiol 10702833Siemens Healthcare Diagnostics Products Ltd · RADIOIMMUNOASSAY, ESTRADIOL1 recall34 reports
- ADVIA Centaur® eE2 10491445Siemens Healthcare Diagnostics Inc. · RADIOIMMUNOASSAY, ESTRADIOL1 recall14 reports
- Elecsys Estradiol III 07027249190Roche Diagnostics GmbH · RADIOIMMUNOASSAY, ESTRADIOL61 reports
- ADVIA Centaur® eE2 10490889Siemens Healthcare Diagnostics Inc. · RADIOIMMUNOASSAY, ESTRADIOL1 recall8 reports
- IMMULITE® 2000 Systems E2 Estradiol 10702834Siemens Healthcare Diagnostics Products Ltd · RADIOIMMUNOASSAY, ESTRADIOL1 recall6 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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