Osom Ultra hCG Combo Test- IVD immunoassay for the qualitative detection of human chorionic gonadotropin (hCG) in serum or urine for the early confirmation of pregnancy. Model/Catalog Number: 1004
Publicado el 6 de noviembre de 2024 · Inicio del retiro: 23 de agosto de 2024
Estado reportado al momento de publicación: Ongoing — openFDA actualiza semanalmente y este campo no refleja el estado más reciente. Confirma siempre con la fuente oficial.
Qué peligro representa
This recall was initiated due to customer complaints of false negative of hCG test results when running patient urine samples. Use of the above listed product lot may result in false negative results. An end user reported that the OSOM Ultra hCG Combo Test, lot 563L13, produced false negative test results from 2 patient urine samples as confirmed by quantitative hCG and ultrasound. During further root cause testing and investigation, an additional 6 devices were found to produce false negative test results from hCG positive samples.
Qué hacer
Voluntary: Firm initiated · Letter
Detalles del retiro
- Fabricante
- Princeton Biomeditech Corp
- Distribuidor
- US Distribution to MO only.
- Lote
- UDI-DI: 00742860100208 Lot Number: 563L13
- Clasificación de riesgo
- Class II
- Área (FDA)
- device
- País
- United States
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