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ARCHITECT
ABBOTT IRELAND · Model 09D9624 · UDI-DI 00380740170189
CZW
Prescription
10
510(k) clearances
3
Adverse events
1
Recalls
31
Facilities
Description
Complement C3 279 Tests
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-05-16 | Abbott Laboratories, Inc | An update to the Reagents and Specimen Collection and Handling/Preparation for Analysis sections of the IFU was required due to different issues with the various products. |
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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.