FDA Device Intelligence
HomeBeckman Coulter, Inc. › IMMAGE

IMMAGE

Beckman Coulter, Inc. · Model 446440 · UDI-DI 15099590230494

DFH Prescription
10
510(k) clearances
55
Adverse events
2
Recalls
18
Facilities

Description

IMMAGE Immunochemistry Systems KAP Kappa Light Chain Reagent

Recalls

DateFirmReason
2021-05-20The Binding Site Group, Ltd.The high and low level "Quality Controls" demonstrate a positive bias of approximately 10% compared to assigned values.
2020-11-18The Binding Site Group, Ltd.Due to customer complaints of positive bias impacting quality control. The high and low level controls are demonstrating a positive bias compared to assigned 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.