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FDA (Device enforcement)Recalled 2024-05-10class ii

Medtronic Neuromodulation: Medtronic Ascenda Intrathecal Catheter, Models: a) 8780 (114 cm); b) 8781 (140 cm); c) 8784 (catheter pump revision kit)

Hazard

Design update to the Ascenda Intrathecal Catheter Models 8780, 8781, and 8784. The intent of the design update is to reduce the potential for tissue growth into the Ascenda catheter connector which may potentially lead to catheter occlusion.

Details from the source

Reason for recall: Design update to the Ascenda Intrathecal Catheter Models 8780, 8781, and 8784. The intent of the design update is to reduce the potential for tissue growth into the Ascenda catheter connector which may potentially lead to catheter occlusion. Distribution: Worldwide Distribution: US (nationwide) and OUS (foreign) countries of: Argentina, Aruba, Australia, Austria, Belgium, Brazil, Canada, Canary Islands, Chile, Colombia, Cyprus, Czech Rep, Denmark, Dominican Republic, Ecuador, Egypt, El Salvador, Estonia, Finland, France, Guadeloupe, Germany, Greece, Hong Kong, Hungary, Indonesia, Italy, Iran, Islamic Republic, Iraq, Ireland, Jordan, Kazakhstan, Kor Quantity: 111762 units Lot/code info: a) 8780: 1) UDI/DI 00643169202122, Lot/Serial Numbers: N690838001, N690838004, N690838005, N690839001, N690839002, N690839003, N690839004, N690839005, N690839006, N690840001, N690840002, N690840003, N690840004, N690840005, N690840006, N690841001, N690841004, N690841005, N690842001, N690842003, N690842004, N690842005, N690843001, N690843003, N690843004, N690843005, N690915002, N690915003, N690915005, N690916001, N690916002, N690916003, N690916005, N690916006, N690917002, N690917003, N690918001, N690918002, N690918003, N690918004, N690918005, N690918006, N690919001, N690919002, N690919003, N690919005, N690919006, N690920001, N690920004, N690920005, N691336003, N691336004, N691336005, N691338001, N691338003, N691338004, N691338005, N691338006, N691456001, N691456002, N691456005, N691461001, N691461002, N691461004, N691461006, N691464002, N691464003, N691464006, N691468001, N691468002, N691468003, N691468005, N691468006, N691479002, N691479003, N691479004, N691479006, N691482001, N691482002, N691482003, N691482004, N691482005, N691506002, N691506003, N691506004, N691508003, N691508004, N691517001, N691517002, N691517004, N691517005, N691522001, N691522002, N691522003, N691522004, N691522005, N691522006, N691524001, N691524002, N691524003, N691524004, N691524005, N691524006, N691527002, N691527003, N691527004, N691527005, N691527006, N691528001, N691528003, N691528004, N691528005, N691528006, N691529002, N691529003, N691529005, N691540001, N691540003, N691540005, N691540006, N6921

UPC codes

00643169202122

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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