Home › Abbott GmbH › Alinity

Alinity

Abbott GmbH · Model 04U7302 · UDI-DI 00380740151294

KRY KRX KSA KRZ Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

ALINITY h-series HemCal

Recalls

Date	Firm	Reason
2006-09-18	Abbott Laboratories	Potential for on-market instability in the whole blood calibrator which could lead to inaccurate platelet (PLT) test results.

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 key Read 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.