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Atellica IM aHCV 200T

Siemens Healthcare Diagnostics Inc. · Model 11207260 · UDI-DI 00630414301341

MZO
0
510(k) clearances
1,679
Adverse events (1 deaths)
7
Recalls
23
Facilities

Description

Atellica IM aHCV 200T Kit

Recalls

DateFirmReason
2024-03-04Abbott GmbHCustomer complaints were received regarding falsely elevated results for some patient samples. Internal studies with customer return samples confirmed potential interactions that m
2024-03-04Abbott GmbHCustomer complaints were received regarding falsely elevated results for some patient samples. Internal studies with customer return samples confirmed potential interactions that m
2016-01-15OraSure Technologies, Inc.OraSure Technologies, Inc. discovered the package insert included with the OraQuick HCV Rapid Antibody test Visual Reference Panel may be incorrect due to a complaint received from
2014-08-06ORTHO-CLINICAL DIAGNOSTICSVITROS Immunodiagnostic Products Anti-HCV kit lot 9090 has been observed producing sporadic lower than expected VITROS Anti-HCV test results due to an approximate signal loss of up
2007-04-23Abbott LaboratoriesFailure of the AxSYM instrument to open (actuate) some reagent packs from certain lots. The defects can result in probe crashes if not detected prior to placement of the reagent k
2006-10-06Home Access Health Corp (HAHC)Wrong Expiration Date; The kits were labeled with Expiration/Use By dates; that exceed the expiration dates of the sterile safety lancet component of the kit.
2004-03-09Diasorin Inc.An error in the acceptance specification for the substrate blank optical density was discovered in the Bio-Tek ELx800 programming specifications for the ORTHO HCV Version 3.0 ELISA

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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.