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Atellica IM T4
Siemens Healthcare Diagnostics Inc. · Model 10995685 · UDI-DI 00630414599984
10
510(k) clearances
100
Adverse events
1
Recalls
13
Facilities
Description
Total T4 (T4) Atellica IM - RGT 750T
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-06-04 | DRG International, Inc. | An incoming complaint reported that the expiration date on the kit box label and Certificate of Analysis (CoA) exceeded the shelf life of the standards and control solutions in the |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
