FDA Device Intelligence
Home › SENTINEL CH. SPA › Albumin BCP (6x20 mL)

Albumin BCP (6x20 mL)

SENTINEL CH. SPA · Model C22855 · UDI-DI 08058056681973

CJW Prescription
10
510(k) clearances
17
Adverse events
1
Recalls
24
Facilities

Description

The Albumin BCP (6x20 mL) assay is an in vitro diagnostic test used for the determination of albumin in human serum or plasma. The assay is intended for professional use only. For In Vitro Diagnostic use only.

Recalls

DateFirmReason
2019-03-18Roche Diagnostics CorporationThe reagent lot is exhibiting calibration failures, QC imprecision, and elevated QC recovery due to elevated pH level causing higher absorbance values.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.