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ADVIA® Chemistry CARB_2 Reagents

Model 10376342 · Siemens Healthcare Diagnostics Inc. · DI 00630414560793

KLT — Enzyme Immunoassay, Carbamazepine · Class II · 21 CFR 862.3645

UDILibrary device dossier · generated 2026-09-15 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.

Recall history (0)

No recalls linked in the loaded window.

Adverse-event reports — MAUDE (0)

Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.

23562019-01: 0 reports for this device; peer average 2/device2019-08: 0 reports for this device; peer average 1/device2019-09: 0 reports for this device; peer average 1/device2019-10: 0 reports for this device; peer average 1/device2019-12: 0 reports for this device; peer average 1/device2020-04: 0 reports for this device; peer average 1/device2021-02: 0 reports for this device; peer average 2/device2022-04: 0 reports for this device; peer average 1/device2022-06: 0 reports for this device; peer average 6/device2023-11: 0 reports for this device; peer average 6/device2024-03: 0 reports for this device; peer average 2/device2025-02: 0 reports for this device; peer average 2/device2025-05: 0 reports for this device; peer average 1.33/device2025-12: 0 reports for this device; peer average 3/device0108091012040204061103020512
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0102
2019-0801
2019-0901
2019-1001
2019-1201
2020-0401
2021-0202
2022-0401
2022-0606
2023-1106
2024-0302
2025-0202
2025-0501.33
2025-1203
This device (reports/month)Average device in KLT (reports/device/month)

Regulatory clearances

  • None linked in the loaded window.

Manufacturer compliance record — Siemens Healthcare Diagnostics Inc.

  • Warning Letter 2012-06-29 Siemens Healthcare Diagnostics, Inc.
  • Warning Letter 2012-06-29 Siemens Healthcare Diagnostics, Inc.
  • Warning Letter 2012-05-29 Siemens Healthcare Diagnostics, Inc.
  • Warning Letter 2012-05-29 Siemens Healthcare Diagnostics, Inc.
  • Warning Letter 2012-05-10 Siemens Healthcare Diagnostics, Inc.
  • Warning Letter 2012-05-10 Siemens Healthcare Diagnostics, Inc.
  • NAI 2026-02-26 Siemens Healthcare Diagnostics Products Ltd. · 0 citations
  • NAI 2024-05-24 Siemens Healthcare Diagnostics, Inc. · 0 citations
  • NAI 2024-05-24 Siemens Healthcare Diagnostics, Inc. · 0 citations
  • NAI 2022-03-30 Siemens Healthcare Diagnostics, Inc. · 0 citations
  • NAI 2022-03-30 Siemens Healthcare Diagnostics, Inc. · 0 citations
  • VAI 2022-03-08 Siemens Healthcare Diagnostics, Inc. · 2 citations
  • VAI 2022-03-08 Siemens Healthcare Diagnostics, Inc. · 2 citations
  • NAI 2021-08-19 Siemens Healthcare Diagnostics Inc · 0 citations
  • NAI 2021-08-19 Siemens Healthcare Diagnostics Inc · 0 citations
  • NAI 2021-03-12 Siemens Healthcare Diagnostics, Inc. · 0 citations
  • NAI 2021-03-12 Siemens Healthcare Diagnostics, Inc. · 0 citations
  • NAI 2019-03-18 Siemens Healthcare Diagnostics Inc. · 0 citations
  • NAI 2018-05-24 Siemens Healthcare Diagnostics Manufacturing Limited · 0 citations
  • VAI 2018-03-02 Siemens Healthcare Diagnostics, Inc. · 4 citations
  • VAI 2018-03-02 Siemens Healthcare Diagnostics, Inc. · 4 citations
  • NAI 2017-11-29 Siemens Healthcare Diagnostics, Inc. · 0 citations
  • NAI 2017-11-29 Siemens Healthcare Diagnostics, Inc. · 0 citations
  • NAI 2017-11-09 Siemens Healthcare Diagnostics Inc · 0 citations
  • NAI 2017-09-26 Siemens Healthcare Diagnostics Inc. · 0 citations
  • NAI 2017-08-25 Siemens Healthcare Diagnostics Inc. · 0 citations