FDA Device Intelligence
HomeAbbott GmbH › Alinity

Alinity

Abbott GmbH · Model 08P2710 · UDI-DI 00380740131364

MJXMJY Prescription
7
510(k) clearances
2
Adverse events
1
Recalls
14
Facilities

Description

Alinity i HAVAb IgG Controls

Recalls

DateFirmReason
2016-06-22Ortho-Clinical DiagnosticsThe signal/cutoff (s/c) results may increase throughout the open-reconstituted timeframe of the allowed 5 days. Increased results may occur on both the negative and positive Contr

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.