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ADS Medical
Model T1-CT30-ADSM · W.H.P.M. INC. · DI 00811925030047
KHE — Reagent, Occult Blood · Class II · 21 CFR 864.6550
UDILibrary device dossier · generated 2026-09-13 · 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.
| Month | This device (reports) | Product-code average (reports per device) |
|---|---|---|
| 2019-08 | 0 | 2 |
| 2020-10 | 0 | 1 |
| 2021-01 | 0 | 2 |
| 2021-07 | 0 | 2 |
| 2021-08 | 0 | 1 |
| 2022-08 | 0 | 1 |
| 2024-03 | 0 | 1 |
| 2025-05 | 0 | 1 |
| 2025-09 | 0 | 1 |
| 2026-05 | 0 | 1 |
Regulatory clearances
- None linked in the loaded window.
Manufacturer compliance record — W.H.P.M. INC.
- Warning Letter 2022-06-30 WHPM Inc.
- Warning Letter 2009-03-19 WHPM Inc.
- VAI 2022-11-18 WHPM Inc. · 3 citations
- OAI 2022-02-28 WHPM Inc. · 0 citations
- NAI 2014-11-13 WHPM Inc. · 0 citations
- NAI 2012-10-31 WHPM Inc. · 0 citations
- VAI 2010-07-01 WHPM Inc. · 0 citations