ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Micro-Introducer Kit, 45CM NT/T NON-ECHO B PG, Item Number H787065970685, Catalog No.REF 06597068, 2) 1) 5 F Stiffened Micro-Introducer Kit, 45CM NT/T NON-ECHO S PG, Item Number H787065970705, Catalog No.REF 06597070 Indicated for percutaneous introduction of guidewire or catheter into the vascular system following a small 21-gauge needle stick
Publicado el 28 de diciembre de 2016 · Inicio del retiro: 28 de septiembre de 2016
Estado reportado al momento de publicación: Terminated — openFDA actualiza semanalmente y este campo no refleja el estado más reciente. Confirma siempre con la fuente oficial.
Qué peligro representa
Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator components has determined that the products listed in their September 7, 2016 Recall Notification have the potential for the rotating luer to detach from the dilator hub during use. AngioDynamics has confirmed that affected sheath/dilators (Greatbatch Model Numbers 10904-001 and 10904-002) have been included in packaged AngioDynamics Stiffened Micro-Introducer Kits.
Qué hacer
Voluntary: Firm initiated · Letter
Detalles del retiro
- Fabricante
- Angiodynamics, Inc.
- Distribuidor
- Nationwide Distribution to AL, AR, CA, FL, GA, IL, KY, LA, MI, MN, MO, NC, OH, OK, SC, NY, ME, PA, MD, VA, WA, WI, WV, TN, and TX
- Lote
- Batch/Lot: 1) 5034280, 5067423, 2) 5061461, 5070972
- Clasificación de riesgo
- Class II
- Área (FDA)
- device
- País
- United States
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