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Atellica IM T4 DIL

Siemens Healthcare Diagnostics Inc. · Model 10995686 · UDI-DI 00630414599991

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

Description

T4 Total (T4) Diluent Bottle Atellica IM - CONS 1 x 10mL

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.