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Atellica IM T4

Siemens Healthcare Diagnostics Inc. · Model 10995685 · UDI-DI 00630414599984

CDX
10
510(k) clearances
100
Adverse events
1
Recalls
13
Facilities

Description

Total T4 (T4) Atellica IM - RGT 750T

Recalls

DateFirmReason
2025-06-04DRG 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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Data 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.