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Alinity
ABBOTT LABORATORIES · Model 06U8101 · UDI-DI 00380740213558
GJH
Prescription
1
510(k) clearances
1
Adverse events
1
Recalls
22
Facilities
Description
RETICULOCYTE REAGENT
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2004-06-24 | ABX Diagnostics Inc | Power failure having impact on software. |
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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.
