RecallRadar

FDA Device recall Z-1897-2019

Siemens Artis zeego--Interventional Fluoroscopic X-Ray System Model Number: 10280959

On 2019-07-10 the FDA classified a Class II recall of Siemens Artis zeego--Interventional Fluoroscopic X-Ray System Model Number: 10280959 by Siemens Medical Solutions Usa, citing artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed connection joining th….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1897-2019
ClassificationClass II
Statusterminated
Initiated2019-06-06
Published2019-07-10
Last updated2026-09-13 11:55 UTC
CompanySiemens Medical Solutions Usa
DistributionUS

Product

Siemens Artis zeego--Interventional Fluoroscopic X-Ray System Model Number: 10280959

Reason

Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed connection joining the pivot bearing to the ceiling-mounted support to work loose or snap off, can result in severe injuries to patients and operating personnel

Identifiers

code_info
Serial Numbers: 160335 160430 160368 160469 160357 160370 160369 160509 160427 160433 160443 160428 160429…Serial Numbers: 160335 160430 160368 160469 160357 160370 160369 160509 160427 160433 160443 160428 160429 160463 160001 160461 160486 160800 160487 160488 160507 160840 160862 160856 160823 160914 160930 161235 160401

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1897-2019%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.